Canonical Allele Identifier: CA419137412

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97305272-A-G
• MyVariant Identifiers: chr1:g.97770828A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305272A>G , CM000663.2:g.97305272A>G	GRCh38
NC_000001.10:g.97770828A>G , CM000663.1:g.97770828A>G	GRCh37
NC_000001.9:g.97543416A>G	NCBI36
NG_008807.2:g.620788T>C , LRG_722:g.620788T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2286T>C (DPYD) MANE Select	ENSP00000359211.3:p.Tyr762=
ENST00000370192.7:c.2286T>C (DPYD)	ENSP00000359211.3:p.Tyr762=
NM_000110.3:c.2286T>C , LRG_722t1:c.2286T>C (DPYD)	NP_000101.2:p.Tyr762=
NR_046590.1:n.129-917A>G (DPYD-AS1)
XM_005270562.3:c.2070T>C (DPYD)	XP_005270619.2:p.Tyr690=
XM_006710397.2:c.2286T>C (DPYD)	XP_006710460.1:p.Tyr762=
XM_006710397.3:c.2286T>C (DPYD)	XP_006710460.1:p.Tyr762=
XM_017000507.1:c.2175T>C (DPYD)	XP_016855996.1:p.Tyr725=
XM_017000508.2:c.1791T>C (DPYD)	XP_016855997.1:p.Tyr597=
XM_017000509.2:c.1791T>C (DPYD)	XP_016855998.1:p.Tyr597=
XM_017000510.1:c.1791T>C (DPYD)	XP_016855999.1:p.Tyr597=
NM_000110.4:c.2286T>C (DPYD) MANE Select	NP_000101.2:p.Tyr762=