Canonical Allele Identifier: CA341379418

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98293696C>G (hg19) ; chr1:g.97828140C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828140C>G , CM000663.2:g.97828140C>G	GRCh38
NC_000001.10:g.98293696C>G , CM000663.1:g.98293696C>G	GRCh37
NC_000001.9:g.98066284C>G	NCBI36
NG_008807.2:g.97920G>C , LRG_722:g.97920G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.207G>C MANE Select	ENSP00000359211.3:p.Glu69Asp
ENST00000306031.5:c.207G>C	ENSP00000307107.5:p.Glu69Asp
ENST00000370192.7:c.207G>C	ENSP00000359211.3:p.Glu69Asp
NM_000110.3:c.207G>C , LRG_722t1:c.207G>C	NP_000101.2:p.Glu69Asp
NM_001160301.1:c.207G>C , LRG_722t2:c.207G>C	NP_001153773.1:p.Glu69Asp
XM_005270562.3:c.207G>C	XP_005270619.2:p.Glu69Asp
XM_006710397.2:c.207G>C	XP_006710460.1:p.Glu69Asp
XM_006710397.3:c.207G>C	XP_006710460.1:p.Glu69Asp
XM_017000507.1:c.96G>C	XP_016855996.1:p.Glu32Asp
XM_017000508.2:c.-504G>C	XP_016855997.1:n.-504G>C
XM_017000509.2:c.-402G>C	XP_016855998.1:n.-402G>C
XM_017000510.1:c.-402G>C	XP_016855999.1:n.-402G>C
XR_001737014.1:n.344G>C
NM_000110.4:c.207G>C MANE Select	NP_000101.2:p.Glu69Asp