Canonical Allele Identifier: CA1241092865

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226991C= , CM000664.2:g.29226991C=	GRCh38
NC_000002.11:g.29449857C= , CM000664.1:g.29449857C=	GRCh37
NC_000002.10:g.29303361C=	NCBI36
NG_009445.1:g.699576G= , LRG_488:g.699576G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2998G= MANE Select	ENSP00000373700.3:p.Glu1000=
ENST00000431873.6:c.164G=
ENST00000389048.7:c.2998G=	ENSP00000373700.3:p.Glu1000=
ENST00000618119.4:c.1867G=	ENSP00000482733.1:p.Glu623=
NM_004304.4:c.2998G=	NP_004295.2:p.Glu1000=
XM_024452778.1:c.151G=	XP_024308546.1:p.Glu51=
XR_001738688.2:n.3854G=
NM_004304.5:c.2998G= MANE Select	NP_004295.2:p.Glu1000=