ClinVar Miner

List of variants in gene ALK reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP
NM_004304.4(ALK):c.-5G>A rs56270786
NM_004304.4(ALK):c.-6G>A rs778056023
NM_004304.4(ALK):c.102G>A (p.Ala34=) rs561278614
NM_004304.4(ALK):c.106C>T (p.Pro36Ser) rs201490095
NM_004304.4(ALK):c.1155-20_1155-19delCT rs140451928
NM_004304.4(ALK):c.1234C>T (p.Arg412Cys) rs147102592
NM_004304.4(ALK):c.1427T>C (p.Val476Ala) rs35093491
NM_004304.4(ALK):c.1464C>T (p.Gly488=) rs56165377
NM_004304.4(ALK):c.1500A>G (p.Gln500=) rs2293564
NM_004304.4(ALK):c.1648-10G>A rs375646347
NM_004304.4(ALK):c.1719C>T (p.Thr573=) rs74830770
NM_004304.4(ALK):c.1752C>T (p.Val584=) rs367912697
NM_004304.4(ALK):c.1753G>A (p.Ala585Thr) rs772496459
NM_004304.4(ALK):c.1817+11T>C rs185559774
NM_004304.4(ALK):c.1943C>T (p.Thr648Ile) rs116202066
NM_004304.4(ALK):c.2039C>T (p.Thr680Ile) rs35228363
NM_004304.4(ALK):c.2148C>T (p.Ser716=) rs55733526
NM_004304.4(ALK):c.2175C>T (p.Ile725=) rs57881134
NM_004304.4(ALK):c.2268C>T (p.Gly756=) rs149853746
NM_004304.4(ALK):c.2451C>T (p.Gly817=) rs183314518
NM_004304.4(ALK):c.2535T>C (p.Gly845=) rs2256740
NM_004304.4(ALK):c.2577G>C (p.Glu859Asp) rs61754865
NM_004304.4(ALK):c.2632+11dup rs766699720
NM_004304.4(ALK):c.2633-4G>A rs199575811
NM_004304.4(ALK):c.2676C>T (p.Ala892=) rs138668699
NM_004304.4(ALK):c.267C>A (p.Gly89=) rs192127241
NM_004304.4(ALK):c.27C>G (p.Leu9=) rs4358080
NM_004304.4(ALK):c.2816-9G>A rs200463420
NM_004304.4(ALK):c.3036G>A (p.Thr1012=) rs2293563
NM_004304.4(ALK):c.3057C>A (p.Val1019=) rs138406372
NM_004304.4(ALK):c.3123C>T (p.Thr1041=) rs773260725
NM_004304.4(ALK):c.3172+12G>C rs1271239593
NM_004304.4(ALK):c.3173-11C>T rs79339096
NM_004304.4(ALK):c.3336G>A (p.Pro1112=) rs146074150
NM_004304.4(ALK):c.3359+6C>T rs4622670
NM_004304.4(ALK):c.3359+7G>A rs778841767
NM_004304.4(ALK):c.3375C>A (p.Gly1125=) rs3795850
NM_004304.4(ALK):c.3375C>T (p.Gly1125=) rs3795850
NM_004304.4(ALK):c.3408C>T (p.Ser1136=) rs56146053
NM_004304.4(ALK):c.3515+18C>T rs79325200
NM_004304.4(ALK):c.3594C>T (p.Leu1198=) rs56071005
NM_004304.4(ALK):c.3742C>T (p.Arg1248Ter) rs145028315
NM_004304.4(ALK):c.3939-8A>G rs3738869
NM_004304.4(ALK):c.4146G>A (p.Arg1382=) rs1553387973
NM_004304.4(ALK):c.4165-6C>T rs17007646
NM_004304.4(ALK):c.4203T>C (p.Tyr1401=) rs55772745
NM_004304.4(ALK):c.4338C>T (p.Thr1446=) rs56132472
NM_004304.4(ALK):c.4381A>G (p.Ile1461Val) rs1670283
NM_004304.4(ALK):c.4472A>G (p.Lys1491Arg) rs1881420
NM_004304.4(ALK):c.4480G>A (p.Gly1494Arg) rs199940609
NM_004304.4(ALK):c.4573_4575delAAG (p.Lys1525del) rs755556501
NM_004304.4(ALK):c.4587C>G (p.Asp1529Glu) rs1881421
NM_004304.4(ALK):c.4596C>T (p.Asn1532=) rs1881422
NM_004304.4(ALK):c.4646G>T (p.Arg1549Ile) rs199646095
NM_004304.4(ALK):c.4785C>T (p.Ala1595=) rs76150405
NM_004304.4(ALK):c.4812C>T (p.Tyr1604=) rs753750497
NM_004304.4(ALK):c.4836G>A (p.Lys1612=) rs78174819
NM_004304.4(ALK):c.4836G>C (p.Lys1612Asn) rs78174819
NM_004304.4(ALK):c.487G>T (p.Val163Leu) rs55697431
NM_004304.4(ALK):c.645T>C (p.Leu215=) rs115392387
NM_004304.4(ALK):c.702T>A (p.Pro234=) rs2246745
NM_004304.4(ALK):c.776G>A (p.Arg259His) rs138686378
NM_004304.4(ALK):c.846C>T (p.Asp282=) rs56116528
NM_004304.4(ALK):c.952+16C>T rs112736234
NM_004304.5(ALK):c.3837-9_3837-7dup rs373764155

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