Canonical Allele Identifier: CA346474409
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667339993

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328436C>A , CM000664.2:g.29328436C>A GRCh38
NC_000002.11:g.29551302C>A , CM000664.1:g.29551302C>A GRCh37
NC_000002.10:g.29404806C>A NCBI36
NG_009445.1:g.598131G>T , LRG_488:g.598131G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1328G>T MANE Select ENSP00000373700.3:p.Cys443Phe
ENST00000389048.7:c.1328G>T ENSP00000373700.3:p.Cys443Phe
ENST00000618119.4:c.197G>T ENSP00000482733.1:p.Cys66Phe
NM_004304.4:c.1328G>T NP_004295.2:p.Cys443Phe
XR_939920.1:n.744C>A
XR_939921.1:n.680+5908C>A
XR_001738688.2:n.2258G>T
XR_939920.2:n.634C>A
XR_939921.2:n.576+5908C>A
NM_004304.5:c.1328G>T MANE Select NP_004295.2:p.Cys443Phe