Canonical Allele Identifier: CA963011

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs672601275
• ExAC: 1:97658715 T / G
• gnomAD v2: 1-97658715-T-G
• MyVariant Identifiers: chr1:g.97658715T>G (hg19) ; chr1:g.97193159T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193159T>G , CM000663.2:g.97193159T>G	GRCh38
NC_000001.10:g.97658715T>G , CM000663.1:g.97658715T>G	GRCh37
NC_000001.9:g.97431303T>G	NCBI36
NG_008807.2:g.732901A>C , LRG_722:g.732901A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2532A>C (DPYD) MANE Select	ENSP00000359211.3:p.Glu844Asp
ENST00000370192.7:c.2532A>C (DPYD)	ENSP00000359211.3:p.Glu844Asp
NM_000110.3:c.2532A>C , LRG_722t1:c.2532A>C (DPYD)	NP_000101.2:p.Glu844Asp
NR_046590.1:n.65-72255T>G (DPYD-AS1)
XM_005270562.3:c.2316A>C (DPYD)	XP_005270619.2:p.Glu772Asp
XM_006710397.2:c.2532A>C (DPYD)	XP_006710460.1:p.Glu844Asp
XM_006710397.3:c.2532A>C (DPYD)	XP_006710460.1:p.Glu844Asp
XM_017000507.1:c.2421A>C (DPYD)	XP_016855996.1:p.Glu807Asp
XM_017000508.2:c.2037A>C (DPYD)	XP_016855997.1:p.Glu679Asp
XM_017000509.2:c.2037A>C (DPYD)	XP_016855998.1:p.Glu679Asp
XM_017000510.1:c.2037A>C (DPYD)	XP_016855999.1:p.Glu679Asp
NM_000110.4:c.2532A>C (DPYD) MANE Select	NP_000101.2:p.Glu844Asp