Canonical Allele Identifier: CA1182839995

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97373595A= , CM000663.2:g.97373595A=	GRCh38
NC_000001.10:g.97839151A= , CM000663.1:g.97839151A=	GRCh37
NC_000001.9:g.97611739A=	NCBI36
NG_008807.2:g.552465T= , LRG_722:g.552465T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2024T= MANE Select	ENSP00000359211.3:p.Met675=
ENST00000370192.7:c.2024T=	ENSP00000359211.3:p.Met675=
NM_000110.3:c.2024T= , LRG_722t1:c.2024T=	NP_000101.2:p.Met675=
XM_005270562.3:c.1808T=	XP_005270619.2:p.Met603=
XM_006710397.2:c.2024T=	XP_006710460.1:p.Met675=
XR_947619.1:n.1125-1933A=
XR_947620.1:n.1124+6394A=
XR_947621.1:n.1125-1933A=
XM_006710397.3:c.2024T=	XP_006710460.1:p.Met675=
XM_017000507.1:c.1913T=	XP_016855996.1:p.Met638=
XM_017000508.2:c.1529T=	XP_016855997.1:p.Met510=
XM_017000509.2:c.1529T=	XP_016855998.1:p.Met510=
XM_017000510.1:c.1529T=	XP_016855999.1:p.Met510=
NM_000110.4:c.2024T= MANE Select	NP_000101.2:p.Met675=