Canonical Allele Identifier: CA346462945

Gene: ALK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3503C>A MANE Select	ENSP00000373700.3:p.Ala1168Asp
ENST00000431873.6:c.730C>A
ENST00000638605.1:n.380C>A
ENST00000642122.1:c.299C>A	ENSP00000493203.1:p.Ala100Asp
ENST00000389048.7:c.3503C>A	ENSP00000373700.3:p.Ala1168Asp
ENST00000431873.5:c.383C>A	ENSP00000414027.2:p.Ala128Asp
ENST00000453137.1:c.197C>A	ENSP00000387488.1:p.Ala66Asp
ENST00000618119.4:c.2372C>A	ENSP00000482733.1:p.Ala791Asp
NM_004304.4:c.3503C>A	NP_004295.2:p.Ala1168Asp
NM_001353765.1:c.299C>A	NP_001340694.1:p.Ala100Asp
XM_024452778.1:c.656C>A	XP_024308546.1:p.Ala219Asp
XM_024452779.1:c.299C>A	XP_024308547.1:p.Ala100Asp
NM_004304.5:c.3503C>A MANE Select	NP_004295.2:p.Ala1168Asp
NM_001353765.2:c.299C>A	NP_001340694.1:p.Ala100Asp