Canonical Allele Identifier: CA346474203

Gene: ALK

Linked Data

• COSMIC: COSM93895
• MyVariant Identifiers: chr2:g.29551256G>C (hg19) ; chr2:g.29328390G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328390G>C , CM000664.2:g.29328390G>C	GRCh38
NC_000002.11:g.29551256G>C , CM000664.1:g.29551256G>C	GRCh37
NC_000002.10:g.29404760G>C	NCBI36
NG_009445.1:g.598177C>G , LRG_488:g.598177C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1374C>G MANE Select	ENSP00000373700.3:p.His458Gln
ENST00000389048.7:c.1374C>G	ENSP00000373700.3:p.His458Gln
ENST00000618119.4:c.243C>G	ENSP00000482733.1:p.His81Gln
NM_004304.4:c.1374C>G	NP_004295.2:p.His458Gln
XR_939920.1:n.698G>C
XR_939921.1:n.680+5862G>C
XR_001738688.2:n.2304C>G
XR_939920.2:n.588G>C
XR_939921.2:n.576+5862G>C
NM_004304.5:c.1374C>G MANE Select	NP_004295.2:p.His458Gln