Canonical Allele Identifier: CA1241083942

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209816C= , CM000664.2:g.29209816C=	GRCh38
NC_000002.11:g.29432682C= , CM000664.1:g.29432682C=	GRCh37
NC_000002.10:g.29286186C=	NCBI36
NG_009445.1:g.716751G= , LRG_488:g.716751G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3806G= MANE Select	ENSP00000373700.3:p.Gly1269=
ENST00000431873.6:c.1033G=
ENST00000638605.1:n.683G=
ENST00000642122.1:c.602G=	ENSP00000493203.1:p.Gly201=
ENST00000389048.7:c.3806G=	ENSP00000373700.3:p.Gly1269=
ENST00000431873.5:c.686G=	ENSP00000414027.2:p.Gly229=
ENST00000618119.4:c.2675G=	ENSP00000482733.1:p.Gly892=
NM_004304.4:c.3806G=	NP_004295.2:p.Gly1269=
NM_001353765.1:c.602G=	NP_001340694.1:p.Gly201=
XM_024452778.1:c.959G=	XP_024308546.1:p.Gly320=
XM_024452779.1:c.602G=	XP_024308547.1:p.Gly201=
NM_004304.5:c.3806G= MANE Select	NP_004295.2:p.Gly1269=
NM_001353765.2:c.602G=	NP_001340694.1:p.Gly201=