Canonical Allele Identifier: CA346474224

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551261A>C (hg19) ; chr2:g.29328395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328395A>C , CM000664.2:g.29328395A>C	GRCh38
NC_000002.11:g.29551261A>C , CM000664.1:g.29551261A>C	GRCh37
NC_000002.10:g.29404765A>C	NCBI36
NG_009445.1:g.598172T>G , LRG_488:g.598172T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1369T>G MANE Select	ENSP00000373700.3:p.Phe457Val
ENST00000389048.7:c.1369T>G	ENSP00000373700.3:p.Phe457Val
ENST00000618119.4:c.238T>G	ENSP00000482733.1:p.Phe80Val
NM_004304.4:c.1369T>G	NP_004295.2:p.Phe457Val
XR_939920.1:n.703A>C
XR_939921.1:n.680+5867A>C
XR_001738688.2:n.2299T>G
XR_939920.2:n.593A>C
XR_939921.2:n.576+5867A>C
NM_004304.5:c.1369T>G MANE Select	NP_004295.2:p.Phe457Val