Canonical Allele Identifier: CA1241144718
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328508T= , CM000664.2:g.29328508T= GRCh38
NC_000002.11:g.29551374T= , CM000664.1:g.29551374T= GRCh37
NC_000002.10:g.29404878T= NCBI36
NG_009445.1:g.598059A= , LRG_488:g.598059A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-27A= MANE Select ENSP00000373700.3:n.1283-27A=
ENST00000389048.7:c.1283-27A= ENSP00000373700.3:n.1283-27A=
ENST00000618119.4:c.152-27A= ENSP00000482733.1:n.152-27A=
NM_004304.4:c.1283-27A= NP_004295.2:n.1283-27A=
XR_939920.1:n.816T=
XR_939921.1:n.680+5980T=
XR_001738688.2:n.2213-27A=
XR_939920.2:n.706T=
XR_939921.2:n.576+5980T=
NM_004304.5:c.1283-27A= MANE Select NP_004295.2:n.1283-27A=