Canonical Allele Identifier: CA419137485

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101036645
• MyVariant Identifiers: chr1:g.97770918A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305362A>T , CM000663.2:g.97305362A>T	GRCh38
NC_000001.10:g.97770918A>T , CM000663.1:g.97770918A>T	GRCh37
NC_000001.9:g.97543506A>T	NCBI36
NG_008807.2:g.620698T>A , LRG_722:g.620698T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2196T>A (DPYD) MANE Select	ENSP00000359211.3:p.Val732=
ENST00000370192.7:c.2196T>A (DPYD)	ENSP00000359211.3:p.Val732=
NM_000110.3:c.2196T>A , LRG_722t1:c.2196T>A (DPYD)	NP_000101.2:p.Val732=
NR_046590.1:n.129-827A>T (DPYD-AS1)
XM_005270562.3:c.1980T>A (DPYD)	XP_005270619.2:p.Val660=
XM_006710397.2:c.2196T>A (DPYD)	XP_006710460.1:p.Val732=
XM_006710397.3:c.2196T>A (DPYD)	XP_006710460.1:p.Val732=
XM_017000507.1:c.2085T>A (DPYD)	XP_016855996.1:p.Val695=
XM_017000508.2:c.1701T>A (DPYD)	XP_016855997.1:p.Val567=
XM_017000509.2:c.1701T>A (DPYD)	XP_016855998.1:p.Val567=
XM_017000510.1:c.1701T>A (DPYD)	XP_016855999.1:p.Val567=
NM_000110.4:c.2196T>A (DPYD) MANE Select	NP_000101.2:p.Val732=