Canonical Allele Identifier: CA346473053

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443627T>C (hg19) ; chr2:g.29220761T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220761T>C , CM000664.2:g.29220761T>C	GRCh38
NC_000002.11:g.29443627T>C , CM000664.1:g.29443627T>C	GRCh37
NC_000002.10:g.29297131T>C	NCBI36
NG_009445.1:g.705806A>G , LRG_488:g.705806A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3590A>G MANE Select	ENSP00000373700.3:p.Glu1197Gly
ENST00000431873.6:c.817A>G
ENST00000638605.1:n.467A>G
ENST00000642122.1:c.386A>G	ENSP00000493203.1:p.Glu129Gly
ENST00000389048.7:c.3590A>G	ENSP00000373700.3:p.Glu1197Gly
ENST00000431873.5:c.470A>G	ENSP00000414027.2:p.Glu157Gly
ENST00000618119.4:c.2459A>G	ENSP00000482733.1:p.Glu820Gly
NM_004304.4:c.3590A>G	NP_004295.2:p.Glu1197Gly
NM_001353765.1:c.386A>G	NP_001340694.1:p.Glu129Gly
XM_024452778.1:c.743A>G	XP_024308546.1:p.Glu248Gly
XM_024452779.1:c.386A>G	XP_024308547.1:p.Glu129Gly
NM_004304.5:c.3590A>G MANE Select	NP_004295.2:p.Glu1197Gly
NM_001353765.2:c.386A>G	NP_001340694.1:p.Glu129Gly