Canonical Allele Identifier: CA341379412

Gene: DPYD

Linked Data

• COSMIC: COSM4980233 ; COSM4980234 ; COSM6190424
• MyVariant Identifiers: chr1:g.98293692C>T (hg19) ; chr1:g.97828136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828136C>T , CM000663.2:g.97828136C>T	GRCh38
NC_000001.10:g.98293692C>T , CM000663.1:g.98293692C>T	GRCh37
NC_000001.9:g.98066280C>T	NCBI36
NG_008807.2:g.97924G>A , LRG_722:g.97924G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.211G>A MANE Select	ENSP00000359211.3:p.Gly71Arg
ENST00000306031.5:c.211G>A	ENSP00000307107.5:p.Gly71Arg
ENST00000370192.7:c.211G>A	ENSP00000359211.3:p.Gly71Arg
NM_000110.3:c.211G>A , LRG_722t1:c.211G>A	NP_000101.2:p.Gly71Arg
NM_001160301.1:c.211G>A , LRG_722t2:c.211G>A	NP_001153773.1:p.Gly71Arg
XM_005270562.3:c.211G>A	XP_005270619.2:p.Gly71Arg
XM_006710397.2:c.211G>A	XP_006710460.1:p.Gly71Arg
XM_006710397.3:c.211G>A	XP_006710460.1:p.Gly71Arg
XM_017000507.1:c.100G>A	XP_016855996.1:p.Gly34Arg
XM_017000508.2:c.-500G>A	XP_016855997.1:n.-500G>A
XM_017000509.2:c.-398G>A	XP_016855998.1:n.-398G>A
XM_017000510.1:c.-398G>A	XP_016855999.1:n.-398G>A
XR_001737014.1:n.348G>A
NM_000110.4:c.211G>A MANE Select	NP_000101.2:p.Gly71Arg