Canonical Allele Identifier: CA341379427

Gene: DPYD

Linked Data

• dbSNP Id: rs1444666147
• gnomAD v2: 1-98293700-C-T
• gnomAD v4: 1-97828144-C-T
• MyVariant Identifiers: chr1:g.98293700C>T (hg19) ; chr1:g.97828144C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828144C>T , CM000663.2:g.97828144C>T	GRCh38
NC_000001.10:g.98293700C>T , CM000663.1:g.98293700C>T	GRCh37
NC_000001.9:g.98066288C>T	NCBI36
NG_008807.2:g.97916G>A , LRG_722:g.97916G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.203G>A MANE Select	ENSP00000359211.3:p.Gly68Asp
ENST00000306031.5:c.203G>A	ENSP00000307107.5:p.Gly68Asp
ENST00000370192.7:c.203G>A	ENSP00000359211.3:p.Gly68Asp
NM_000110.3:c.203G>A , LRG_722t1:c.203G>A	NP_000101.2:p.Gly68Asp
NM_001160301.1:c.203G>A , LRG_722t2:c.203G>A	NP_001153773.1:p.Gly68Asp
XM_005270562.3:c.203G>A	XP_005270619.2:p.Gly68Asp
XM_006710397.2:c.203G>A	XP_006710460.1:p.Gly68Asp
XM_006710397.3:c.203G>A	XP_006710460.1:p.Gly68Asp
XM_017000507.1:c.92G>A	XP_016855996.1:p.Gly31Asp
XM_017000508.2:c.-508G>A	XP_016855997.1:n.-508G>A
XM_017000509.2:c.-406G>A	XP_016855998.1:n.-406G>A
XM_017000510.1:c.-406G>A	XP_016855999.1:n.-406G>A
XR_001737014.1:n.340G>A
NM_000110.4:c.203G>A MANE Select	NP_000101.2:p.Gly68Asp