Canonical Allele Identifier: CA1182758315

Gene: DPYD DPYD-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193299C= , CM000663.2:g.97193299C=	GRCh38
NC_000001.10:g.97658855C= , CM000663.1:g.97658855C=	GRCh37
NC_000001.9:g.97431443C=	NCBI36
NG_008807.2:g.732761G= , LRG_722:g.732761G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2443-51G= (DPYD) MANE Select	ENSP00000359211.3:n.2443-51G=
ENST00000370192.7:c.2443-51G= (DPYD)	ENSP00000359211.3:n.2443-51G=
NM_000110.3:c.2443-51G= , LRG_722t1:c.2443-51G= (DPYD)	NP_000101.2:n.2443-51G=
NR_046590.1:n.65-72115C= (DPYD-AS1)
XM_005270562.3:c.2227-51G= (DPYD)	XP_005270619.2:n.2227-51G=
XM_006710397.2:c.2443-51G= (DPYD)	XP_006710460.1:n.2443-51G=
XM_006710397.3:c.2443-51G= (DPYD)	XP_006710460.1:n.2443-51G=
XM_017000507.1:c.2332-51G= (DPYD)	XP_016855996.1:n.2332-51G=
XM_017000508.2:c.1948-51G= (DPYD)	XP_016855997.1:n.1948-51G=
XM_017000509.2:c.1948-51G= (DPYD)	XP_016855998.1:n.1948-51G=
XM_017000510.1:c.1948-51G= (DPYD)	XP_016855999.1:n.1948-51G=
NM_000110.4:c.2443-51G= (DPYD) MANE Select	NP_000101.2:n.2443-51G=