Canonical Allele Identifier: CA346473156

Gene: ALK

Linked Data

• dbSNP Id: rs1198494888
• MyVariant Identifiers: chr2:g.29443682T>A (hg19) ; chr2:g.29220816T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220816T>A , CM000664.2:g.29220816T>A	GRCh38
NC_000002.11:g.29443682T>A , CM000664.1:g.29443682T>A	GRCh37
NC_000002.10:g.29297186T>A	NCBI36
NG_009445.1:g.705751A>T , LRG_488:g.705751A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3535A>T MANE Select	ENSP00000373700.3:p.Ile1179Phe
ENST00000431873.6:c.762A>T
ENST00000638605.1:n.412A>T
ENST00000642122.1:c.331A>T	ENSP00000493203.1:p.Ile111Phe
ENST00000389048.7:c.3535A>T	ENSP00000373700.3:p.Ile1179Phe
ENST00000431873.5:c.415A>T	ENSP00000414027.2:p.Ile139Phe
ENST00000618119.4:c.2404A>T	ENSP00000482733.1:p.Ile802Phe
NM_004304.4:c.3535A>T	NP_004295.2:p.Ile1179Phe
NM_001353765.1:c.331A>T	NP_001340694.1:p.Ile111Phe
XM_024452778.1:c.688A>T	XP_024308546.1:p.Ile230Phe
XM_024452779.1:c.331A>T	XP_024308547.1:p.Ile111Phe
NM_004304.5:c.3535A>T MANE Select	NP_004295.2:p.Ile1179Phe
NM_001353765.2:c.331A>T	NP_001340694.1:p.Ile111Phe