Canonical Allele Identifier: CA346474397

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551300A>G (hg19) ; chr2:g.29328434A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328434A>G , CM000664.2:g.29328434A>G	GRCh38
NC_000002.11:g.29551300A>G , CM000664.1:g.29551300A>G	GRCh37
NC_000002.10:g.29404804A>G	NCBI36
NG_009445.1:g.598133T>C , LRG_488:g.598133T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1330T>C MANE Select	ENSP00000373700.3:p.Trp444Arg
ENST00000389048.7:c.1330T>C	ENSP00000373700.3:p.Trp444Arg
ENST00000618119.4:c.199T>C	ENSP00000482733.1:p.Trp67Arg
NM_004304.4:c.1330T>C	NP_004295.2:p.Trp444Arg
XR_939920.1:n.742A>G
XR_939921.1:n.680+5906A>G
XR_001738688.2:n.2260T>C
XR_939920.2:n.632A>G
XR_939921.2:n.576+5906A>G
NM_004304.5:c.1330T>C MANE Select	NP_004295.2:p.Trp444Arg