Canonical Allele Identifier: CA1241144714
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667342779

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328505C>A , CM000664.2:g.29328505C>A GRCh38
NC_000002.11:g.29551371C>A , CM000664.1:g.29551371C>A GRCh37
NC_000002.10:g.29404875C>A NCBI36
NG_009445.1:g.598062G>T , LRG_488:g.598062G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-24G>T MANE Select ENSP00000373700.3:n.1283-24G>T
ENST00000389048.7:c.1283-24G>T ENSP00000373700.3:n.1283-24G>T
ENST00000618119.4:c.152-24G>T ENSP00000482733.1:n.152-24G>T
NM_004304.4:c.1283-24G>T NP_004295.2:n.1283-24G>T
XR_939920.1:n.813C>A
XR_939921.1:n.680+5977C>A
XR_001738688.2:n.2213-24G>T
XR_939920.2:n.703C>A
XR_939921.2:n.576+5977C>A
NM_004304.5:c.1283-24G>T MANE Select NP_004295.2:n.1283-24G>T