Canonical Allele Identifier: CA1241144697
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328489G= , CM000664.2:g.29328489G= GRCh38
NC_000002.11:g.29551355G= , CM000664.1:g.29551355G= GRCh37
NC_000002.10:g.29404859G= NCBI36
NG_009445.1:g.598078C= , LRG_488:g.598078C=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-8C= MANE Select ENSP00000373700.3:n.1283-8C=
ENST00000389048.7:c.1283-8C= ENSP00000373700.3:n.1283-8C=
ENST00000618119.4:c.152-8C= ENSP00000482733.1:n.152-8C=
NM_004304.4:c.1283-8C= NP_004295.2:n.1283-8C=
XR_939920.1:n.797G=
XR_939921.1:n.680+5961G=
XR_001738688.2:n.2213-8C=
XR_939920.2:n.687G=
XR_939921.2:n.576+5961G=
NM_004304.5:c.1283-8C= MANE Select NP_004295.2:n.1283-8C=