Canonical Allele Identifier: CA346462932

Gene: ALK

Linked Data

• dbSNP Id: rs2148168589
• MyVariant Identifiers: chr2:g.29445222G>A (hg19) ; chr2:g.29222356G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222356G>A , CM000664.2:g.29222356G>A	GRCh38
NC_000002.11:g.29445222G>A , CM000664.1:g.29445222G>A	GRCh37
NC_000002.10:g.29298726G>A	NCBI36
NG_009445.1:g.704211C>T , LRG_488:g.704211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3503C>T MANE Select	ENSP00000373700.3:p.Ala1168Val
ENST00000431873.6:c.730C>T
ENST00000638605.1:n.380C>T
ENST00000642122.1:c.299C>T	ENSP00000493203.1:p.Ala100Val
ENST00000389048.7:c.3503C>T	ENSP00000373700.3:p.Ala1168Val
ENST00000431873.5:c.383C>T	ENSP00000414027.2:p.Ala128Val
ENST00000453137.1:c.197C>T	ENSP00000387488.1:p.Ala66Val
ENST00000618119.4:c.2372C>T	ENSP00000482733.1:p.Ala791Val
NM_004304.4:c.3503C>T	NP_004295.2:p.Ala1168Val
NM_001353765.1:c.299C>T	NP_001340694.1:p.Ala100Val
XM_024452778.1:c.656C>T	XP_024308546.1:p.Ala219Val
XM_024452779.1:c.299C>T	XP_024308547.1:p.Ala100Val
NM_004304.5:c.3503C>T MANE Select	NP_004295.2:p.Ala1168Val
NM_001353765.2:c.299C>T	NP_001340694.1:p.Ala100Val