Canonical Allele Identifier: CA1182843800

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382535C= , CM000663.2:g.97382535C=	GRCh38
NC_000001.10:g.97848091C= , CM000663.1:g.97848091C=	GRCh37
NC_000001.9:g.97620679C=	NCBI36
NG_008807.2:g.543525G= , LRG_722:g.543525G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-74G= MANE Select	ENSP00000359211.3:n.1906-74G=
ENST00000370192.7:c.1906-74G=	ENSP00000359211.3:n.1906-74G=
NM_000110.3:c.1906-74G= , LRG_722t1:c.1906-74G=	NP_000101.2:n.1906-74G=
XM_005270562.3:c.1690-74G=	XP_005270619.2:n.1690-74G=
XM_006710397.2:c.1906-74G=	XP_006710460.1:n.1906-74G=
XR_947619.1:n.1347-1099C=
XR_947620.1:n.1125-1099C=
XR_947621.1:n.1347-1099C=
XM_006710397.3:c.1906-74G=	XP_006710460.1:n.1906-74G=
XM_017000507.1:c.1795-74G=	XP_016855996.1:n.1795-74G=
XM_017000508.2:c.1411-74G=	XP_016855997.1:n.1411-74G=
XM_017000509.2:c.1411-74G=	XP_016855998.1:n.1411-74G=
XM_017000510.1:c.1411-74G=	XP_016855999.1:n.1411-74G=
XR_001737686.2:n.692-1099C=
XR_001737687.1:n.692-1099C=
XR_001737688.2:n.692-1099C=
NM_000110.4:c.1906-74G= MANE Select	NP_000101.2:n.1906-74G=