Canonical Allele Identifier: CA1241144843
Gene: ALK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328627G= , CM000664.2:g.29328627G= GRCh38
NC_000002.11:g.29551493G= , CM000664.1:g.29551493G= GRCh37
NC_000002.10:g.29404997G= NCBI36
NG_009445.1:g.597940C= , LRG_488:g.597940C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-146C= MANE Select ENSP00000373700.3:n.1283-146C=
ENST00000389048.7:c.1283-146C= ENSP00000373700.3:n.1283-146C=
ENST00000618119.4:c.152-146C= ENSP00000482733.1:n.152-146C=
NM_004304.4:c.1283-146C= NP_004295.2:n.1283-146C=
XR_939920.1:n.817+118G=
XR_939921.1:n.680+6099G=
XR_001738688.2:n.2213-146C=
XR_939920.2:n.707+118G=
XR_939921.2:n.576+6099G=
NM_004304.5:c.1283-146C= MANE Select NP_004295.2:n.1283-146C=
Search 100 bp 5'
Search 100 bp 3'