Canonical Allele Identifier: CA1241144539

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328389G= , CM000664.2:g.29328389G=	GRCh38
NC_000002.11:g.29551255G= , CM000664.1:g.29551255G=	GRCh37
NC_000002.10:g.29404759G=	NCBI36
NG_009445.1:g.598178C= , LRG_488:g.598178C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1375C= MANE Select	ENSP00000373700.3:p.Gln459=
ENST00000389048.7:c.1375C=	ENSP00000373700.3:p.Gln459=
ENST00000618119.4:c.244C=	ENSP00000482733.1:p.Gln82=
NM_004304.4:c.1375C=	NP_004295.2:p.Gln459=
XR_939920.1:n.697G=
XR_939921.1:n.680+5861G=
XR_001738688.2:n.2305C=
XR_939920.2:n.587G=
XR_939921.2:n.576+5861G=
NM_004304.5:c.1375C= MANE Select	NP_004295.2:p.Gln459=