Canonical Allele Identifier: CA346474222

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29551260A>T (hg19) ; chr2:g.29328394A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328394A>T , CM000664.2:g.29328394A>T	GRCh38
NC_000002.11:g.29551260A>T , CM000664.1:g.29551260A>T	GRCh37
NC_000002.10:g.29404764A>T	NCBI36
NG_009445.1:g.598173T>A , LRG_488:g.598173T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.1370T>A MANE Select	ENSP00000373700.3:p.Phe457Tyr
ENST00000389048.7:c.1370T>A	ENSP00000373700.3:p.Phe457Tyr
ENST00000618119.4:c.239T>A	ENSP00000482733.1:p.Phe80Tyr
NM_004304.4:c.1370T>A	NP_004295.2:p.Phe457Tyr
XR_939920.1:n.702A>T
XR_939921.1:n.680+5866A>T
XR_001738688.2:n.2300T>A
XR_939920.2:n.592A>T
XR_939921.2:n.576+5866A>T
NM_004304.5:c.1370T>A MANE Select	NP_004295.2:p.Phe457Tyr