Canonical Allele Identifier: CA645528800

Gene: ALK

Linked Data

• dbSNP Id: rs2148168531
• COSMIC: COSM1169448

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222346_29222347delinsAT , CM000664.2:g.29222346_29222347delinsAT	GRCh38
NC_000002.11:g.29445212_29445213delinsAT , CM000664.1:g.29445212_29445213delinsAT	GRCh37
NC_000002.10:g.29298716_29298717delinsAT	NCBI36
NG_009445.1:g.704220_704221delinsAT , LRG_488:g.704220_704221delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3512_3513delinsAT MANE Select	ENSP00000373700.3:p.Ile1171Asn
ENST00000431873.6:c.739_740delinsAT
ENST00000638605.1:n.389_390delinsAT
ENST00000642122.1:c.308_309delinsAT	ENSP00000493203.1:p.Ile103Asn
ENST00000389048.7:c.3512_3513delinsAT	ENSP00000373700.3:p.Ile1171Asn
ENST00000431873.5:c.392_393delinsAT	ENSP00000414027.2:p.Ile131Asn
ENST00000453137.1:c.206_207delinsAT	ENSP00000387488.1:p.Ile69Asn
ENST00000618119.4:c.2381_2382delinsAT	ENSP00000482733.1:p.Ile794Asn
NM_004304.4:c.3512_3513delinsAT	NP_004295.2:p.Ile1171Asn
NM_001353765.1:c.308_309delinsAT	NP_001340694.1:p.Ile103Asn
XM_024452778.1:c.665_666delinsAT	XP_024308546.1:p.Ile222Asn
XM_024452779.1:c.308_309delinsAT	XP_024308547.1:p.Ile103Asn
NM_004304.5:c.3512_3513delinsAT MANE Select	NP_004295.2:p.Ile1171Asn
NM_001353765.2:c.308_309delinsAT	NP_001340694.1:p.Ile103Asn