Canonical Allele Identifier: CA1182979318

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691769G= , CM000663.2:g.97691769G=	GRCh38
NC_000001.10:g.98157325G= , CM000663.1:g.98157325G=	GRCh37
NC_000001.9:g.97929913G=	NCBI36
NG_008807.2:g.234291C= , LRG_722:g.234291C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.710C= MANE Select	ENSP00000359211.3:p.Pro237=
ENST00000370192.7:c.710C=	ENSP00000359211.3:p.Pro237=
ENST00000474241.1:n.474C=
NM_000110.3:c.710C= , LRG_722t1:c.710C=	NP_000101.2:p.Pro237=
XM_005270562.3:c.710C=	XP_005270619.2:p.Pro237=
XM_006710397.2:c.710C=	XP_006710460.1:p.Pro237=
XM_006710397.3:c.710C=	XP_006710460.1:p.Pro237=
XM_017000507.1:c.599C=	XP_016855996.1:p.Pro200=
XM_017000508.2:c.215C=	XP_016855997.1:p.Pro72=
XM_017000509.2:c.215C=	XP_016855998.1:p.Pro72=
XM_017000510.1:c.215C=	XP_016855999.1:p.Pro72=
NM_000110.4:c.710C= MANE Select	NP_000101.2:p.Pro237=