Canonical Allele Identifier: CA1241144528
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328386C= , CM000664.2:g.29328386C= GRCh38
NC_000002.11:g.29551252C= , CM000664.1:g.29551252C= GRCh37
NC_000002.10:g.29404756C= NCBI36
NG_009445.1:g.598181G= , LRG_488:g.598181G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1378G= MANE Select ENSP00000373700.3:p.Asp460=
ENST00000389048.7:c.1378G= ENSP00000373700.3:p.Asp460=
ENST00000618119.4:c.247G= ENSP00000482733.1:p.Asp83=
NM_004304.4:c.1378G= NP_004295.2:p.Asp460=
XR_939920.1:n.694C=
XR_939921.1:n.680+5858C=
XR_001738688.2:n.2308G=
XR_939920.2:n.584C=
XR_939921.2:n.576+5858C=
NM_004304.5:c.1378G= MANE Select NP_004295.2:p.Asp460=