Canonical Allele Identifier: CA341373465

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97193160-T-G
• MyVariant Identifiers: chr1:g.97658716T>G (hg19) ; chr1:g.97193160T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193160T>G , CM000663.2:g.97193160T>G	GRCh38
NC_000001.10:g.97658716T>G , CM000663.1:g.97658716T>G	GRCh37
NC_000001.9:g.97431304T>G	NCBI36
NG_008807.2:g.732900A>C , LRG_722:g.732900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2531A>C (DPYD) MANE Select	ENSP00000359211.3:p.Glu844Ala
ENST00000370192.7:c.2531A>C (DPYD)	ENSP00000359211.3:p.Glu844Ala
NM_000110.3:c.2531A>C , LRG_722t1:c.2531A>C (DPYD)	NP_000101.2:p.Glu844Ala
NR_046590.1:n.65-72254T>G (DPYD-AS1)
XM_005270562.3:c.2315A>C (DPYD)	XP_005270619.2:p.Glu772Ala
XM_006710397.2:c.2531A>C (DPYD)	XP_006710460.1:p.Glu844Ala
XM_006710397.3:c.2531A>C (DPYD)	XP_006710460.1:p.Glu844Ala
XM_017000507.1:c.2420A>C (DPYD)	XP_016855996.1:p.Glu807Ala
XM_017000508.2:c.2036A>C (DPYD)	XP_016855997.1:p.Glu679Ala
XM_017000509.2:c.2036A>C (DPYD)	XP_016855998.1:p.Glu679Ala
XM_017000510.1:c.2036A>C (DPYD)	XP_016855999.1:p.Glu679Ala
NM_000110.4:c.2531A>C (DPYD) MANE Select	NP_000101.2:p.Glu844Ala