Canonical Allele Identifier: CA1146437582

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97883172A= , CM000663.2:g.97883172A=	GRCh38
NC_000001.10:g.98348728A= , CM000663.1:g.98348728A=	GRCh37
NC_000001.9:g.98121316A=	NCBI36
NG_008807.2:g.42888T= , LRG_722:g.42888T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.150+92T= MANE Select	ENSP00000359211.3:n.150+92T=
ENST00000306031.5:c.150+92T=	ENSP00000307107.5:n.150+92T=
ENST00000370192.7:c.150+92T=	ENSP00000359211.3:n.150+92T=
ENST00000460019.1:n.225+92T=
NM_000110.3:c.150+92T= , LRG_722t1:c.150+92T=	NP_000101.2:n.150+92T=
NM_001160301.1:c.150+92T= , LRG_722t2:c.150+92T=	NP_001153773.1:n.150+92T=
XM_005270562.3:c.150+92T=	XP_005270619.2:n.150+92T=
XM_006710397.2:c.150+92T=	XP_006710460.1:n.150+92T=
XM_006710397.3:c.150+92T=	XP_006710460.1:n.150+92T=
XM_017000507.1:c.39+37712T=	XP_016855996.1:n.39+37712T=
XM_017000508.2:c.-561+92T=	XP_016855997.1:n.-561+92T=
XM_017000509.2:c.-459+92T=	XP_016855998.1:n.-459+92T=
XM_017000510.1:c.-459+37712T=	XP_016855999.1:n.-459+37712T=
XR_001737014.1:n.287+92T=
NM_000110.4:c.150+92T= MANE Select	NP_000101.2:n.150+92T=