Canonical Allele Identifier: CA346463136

Gene: ALK

Linked Data

• dbSNP Id: rs2148168656
• MyVariant Identifiers: chr2:g.29445246T>A (hg19) ; chr2:g.29222380T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222380T>A , CM000664.2:g.29222380T>A	GRCh38
NC_000002.11:g.29445246T>A , CM000664.1:g.29445246T>A	GRCh37
NC_000002.10:g.29298750T>A	NCBI36
NG_009445.1:g.704187A>T , LRG_488:g.704187A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3479A>T MANE Select	ENSP00000373700.3:p.Asp1160Val
ENST00000431873.6:c.706A>T
ENST00000638605.1:n.356A>T
ENST00000642122.1:c.275A>T	ENSP00000493203.1:p.Asp92Val
ENST00000389048.7:c.3479A>T	ENSP00000373700.3:p.Asp1160Val
ENST00000431873.5:c.359A>T	ENSP00000414027.2:p.Asp120Val
ENST00000453137.1:c.173A>T	ENSP00000387488.1:p.Asp58Val
ENST00000618119.4:c.2348A>T	ENSP00000482733.1:p.Asp783Val
NM_004304.4:c.3479A>T	NP_004295.2:p.Asp1160Val
NM_001353765.1:c.275A>T	NP_001340694.1:p.Asp92Val
XM_024452778.1:c.632A>T	XP_024308546.1:p.Asp211Val
XM_024452779.1:c.275A>T	XP_024308547.1:p.Asp92Val
NM_004304.5:c.3479A>T MANE Select	NP_004295.2:p.Asp1160Val
NM_001353765.2:c.275A>T	NP_001340694.1:p.Asp92Val