Canonical Allele Identifier: CA2573134582
Gene: ALK HGNC NCBI

Linked Data

ClinVar Variation Id: 1636479
ClinVar RCV Id: RCV002128394
dbSNP Id: rs2148258457

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328493A>G , CM000664.2:g.29328493A>G GRCh38
NC_000002.11:g.29551359A>G , CM000664.1:g.29551359A>G GRCh37
NC_000002.10:g.29404863A>G NCBI36
NG_009445.1:g.598074T>C , LRG_488:g.598074T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-12T>C MANE Select ENSP00000373700.3:n.1283-12T>C
ENST00000389048.7:c.1283-12T>C ENSP00000373700.3:n.1283-12T>C
ENST00000618119.4:c.152-12T>C ENSP00000482733.1:n.152-12T>C
NM_004304.4:c.1283-12T>C NP_004295.2:n.1283-12T>C
XR_939920.1:n.801A>G
XR_939921.1:n.680+5965A>G
XR_001738688.2:n.2213-12T>C
XR_939920.2:n.691A>G
XR_939921.2:n.576+5965A>G
NM_004304.5:c.1283-12T>C MANE Select NP_004295.2:n.1283-12T>C