Canonical Allele Identifier: CA1241144957
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328773_29328774delinsCG , CM000664.2:g.29328773_29328774delinsCG GRCh38
NC_000002.11:g.29551639_29551640delinsCG , CM000664.1:g.29551639_29551640delinsCG GRCh37
NC_000002.10:g.29405143_29405144delinsCG NCBI36
NG_009445.1:g.597793_597794delinsCG , LRG_488:g.597793_597794delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-293_1283-292delinsCG MANE Select ENSP00000373700.3:n.1283-293_1283-292delinsCG
ENST00000389048.7:c.1283-293_1283-292delinsCG ENSP00000373700.3:n.1283-293_1283-292delinsCG
ENST00000618119.4:c.152-293_152-292delinsCG ENSP00000482733.1:n.152-293_152-292delinsCG
NM_004304.4:c.1283-293_1283-292delinsCG NP_004295.2:n.1283-293_1283-292delinsCG
XR_939920.1:n.818-152_818-151delinsCG
XR_939921.1:n.680+6245_680+6246delinsCG
XR_001738688.2:n.2213-293_2213-292delinsCG
XR_939920.2:n.708-152_708-151delinsCG
XR_939921.2:n.576+6245_576+6246delinsCG
NM_004304.5:c.1283-293_1283-292delinsCG MANE Select NP_004295.2:n.1283-293_1283-292delinsCG