Canonical Allele Identifier: CA1182979101

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691228A= , CM000663.2:g.97691228A=	GRCh38
NC_000001.10:g.98156784A= , CM000663.1:g.98156784A=	GRCh37
NC_000001.9:g.97929372A=	NCBI36
NG_008807.2:g.234832T= , LRG_722:g.234832T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+489T= MANE Select	ENSP00000359211.3:n.762+489T=
ENST00000370192.7:c.762+489T=	ENSP00000359211.3:n.762+489T=
ENST00000474241.1:n.1015T=
NM_000110.3:c.762+489T= , LRG_722t1:c.762+489T=	NP_000101.2:n.762+489T=
XM_005270562.3:c.762+489T=	XP_005270619.2:n.762+489T=
XM_006710397.2:c.762+489T=	XP_006710460.1:n.762+489T=
XM_006710397.3:c.762+489T=	XP_006710460.1:n.762+489T=
XM_017000507.1:c.651+489T=	XP_016855996.1:n.651+489T=
XM_017000508.2:c.267+489T=	XP_016855997.1:n.267+489T=
XM_017000509.2:c.267+489T=	XP_016855998.1:n.267+489T=
XM_017000510.1:c.267+489T=	XP_016855999.1:n.267+489T=
NM_000110.4:c.762+489T= MANE Select	NP_000101.2:n.762+489T=