Canonical Allele Identifier: CA1141963075

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97740439G= , CM000663.2:g.97740439G=	GRCh38
NC_000001.10:g.98205995G= , CM000663.1:g.98205995G=	GRCh37
NC_000001.9:g.97978583G=	NCBI36
NG_008807.2:g.185621C= , LRG_722:g.185621C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.274C= MANE Select	ENSP00000359211.3:p.Pro92=
ENST00000306031.5:c.274C=	ENSP00000307107.5:p.Pro92=
ENST00000370192.7:c.274C=	ENSP00000359211.3:p.Pro92=
NM_000110.3:c.274C= , LRG_722t1:c.274C=	NP_000101.2:p.Pro92=
NM_001160301.1:c.274C= , LRG_722t2:c.274C=	NP_001153773.1:p.Pro92=
XM_005270562.3:c.274C=	XP_005270619.2:p.Pro92=
XM_006710397.2:c.274C=	XP_006710460.1:p.Pro92=
XM_006710397.3:c.274C=	XP_006710460.1:p.Pro92=
XM_017000507.1:c.163C=	XP_016855996.1:p.Pro55=
XM_017000508.2:c.-437C=	XP_016855997.1:n.-437C=
XM_017000509.2:c.-335C=	XP_016855998.1:n.-335C=
XM_017000510.1:c.-335C=	XP_016855999.1:n.-335C=
XR_001737014.1:n.411C=
NM_000110.4:c.274C= MANE Select	NP_000101.2:p.Pro92=