Canonical Allele Identifier: CA1182979311

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691752A= , CM000663.2:g.97691752A=	GRCh38
NC_000001.10:g.98157308A= , CM000663.1:g.98157308A=	GRCh37
NC_000001.9:g.97929896A=	NCBI36
NG_008807.2:g.234308T= , LRG_722:g.234308T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.727T= MANE Select	ENSP00000359211.3:p.Phe243=
ENST00000370192.7:c.727T=	ENSP00000359211.3:p.Phe243=
ENST00000474241.1:n.491T=
NM_000110.3:c.727T= , LRG_722t1:c.727T=	NP_000101.2:p.Phe243=
XM_005270562.3:c.727T=	XP_005270619.2:p.Phe243=
XM_006710397.2:c.727T=	XP_006710460.1:p.Phe243=
XM_006710397.3:c.727T=	XP_006710460.1:p.Phe243=
XM_017000507.1:c.616T=	XP_016855996.1:p.Phe206=
XM_017000508.2:c.232T=	XP_016855997.1:p.Phe78=
XM_017000509.2:c.232T=	XP_016855998.1:p.Phe78=
XM_017000510.1:c.232T=	XP_016855999.1:p.Phe78=
NM_000110.4:c.727T= MANE Select	NP_000101.2:p.Phe243=