Canonical Allele Identifier: CA1241144545
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328390G= , CM000664.2:g.29328390G= GRCh38
NC_000002.11:g.29551256G= , CM000664.1:g.29551256G= GRCh37
NC_000002.10:g.29404760G= NCBI36
NG_009445.1:g.598177C= , LRG_488:g.598177C=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1374C= MANE Select ENSP00000373700.3:p.His458=
ENST00000389048.7:c.1374C= ENSP00000373700.3:p.His458=
ENST00000618119.4:c.243C= ENSP00000482733.1:p.His81=
NM_004304.4:c.1374C= NP_004295.2:p.His458=
XR_939920.1:n.698G=
XR_939921.1:n.680+5862G=
XR_001738688.2:n.2304C=
XR_939920.2:n.588G=
XR_939921.2:n.576+5862G=
NM_004304.5:c.1374C= MANE Select NP_004295.2:p.His458=