Canonical Allele Identifier: CA2696573836

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101035989

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305304del , CM000663.2:g.97305304del	GRCh38
NC_000001.10:g.97770860del , CM000663.1:g.97770860del	GRCh37
NC_000001.9:g.97543448del	NCBI36
NG_008807.2:g.620757del , LRG_722:g.620757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2255del (DPYD) MANE Select	ENSP00000359211.3:p.Pro752GlnfsTer24
ENST00000370192.7:c.2255del (DPYD)	ENSP00000359211.3:p.Pro752GlnfsTer24
NM_000110.3:c.2255del , LRG_722t1:c.2255del (DPYD)	NP_000101.2:p.Pro752GlnfsTer24
NR_046590.1:n.129-885del (DPYD-AS1)
XM_005270562.3:c.2039del (DPYD)	XP_005270619.2:p.Pro680GlnfsTer24
XM_006710397.2:c.2255del (DPYD)	XP_006710460.1:p.Pro752GlnfsTer24
XM_006710397.3:c.2255del (DPYD)	XP_006710460.1:p.Pro752GlnfsTer24
XM_017000507.1:c.2144del (DPYD)	XP_016855996.1:p.Pro715GlnfsTer24
XM_017000508.2:c.1760del (DPYD)	XP_016855997.1:p.Pro587GlnfsTer24
XM_017000509.2:c.1760del (DPYD)	XP_016855998.1:p.Pro587GlnfsTer24
XM_017000510.1:c.1760del (DPYD)	XP_016855999.1:p.Pro587GlnfsTer24
NM_000110.4:c.2255del (DPYD) MANE Select	NP_000101.2:p.Pro752GlnfsTer24