Canonical Allele Identifier: CA1241144717
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs1667342942
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-27A>T MANE Select ENSP00000373700.3:n.1283-27A>T
ENST00000389048.7:c.1283-27A>T ENSP00000373700.3:n.1283-27A>T
ENST00000618119.4:c.152-27A>T ENSP00000482733.1:n.152-27A>T
NM_004304.4:c.1283-27A>T NP_004295.2:n.1283-27A>T
XR_939920.1:n.816T>A
XR_939921.1:n.680+5980T>A
XR_001738688.2:n.2213-27A>T
XR_939920.2:n.706T>A
XR_939921.2:n.576+5980T>A
NM_004304.5:c.1283-27A>T MANE Select NP_004295.2:n.1283-27A>T
Search 100 bp 5'
Search 100 bp 3'