Canonical Allele Identifier: CA341375019

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1667087892
• gnomAD v3: 1-97305265-C-T
• gnomAD v4: 1-97305265-C-T
• MyVariant Identifiers: chr1:g.97770821C>T (hg19) ; chr1:g.97305265C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305265C>T , CM000663.2:g.97305265C>T	GRCh38
NC_000001.10:g.97770821C>T , CM000663.1:g.97770821C>T	GRCh37
NC_000001.9:g.97543409C>T	NCBI36
NG_008807.2:g.620795G>A , LRG_722:g.620795G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2293G>A (DPYD) MANE Select	ENSP00000359211.3:p.Val765Met
ENST00000370192.7:c.2293G>A (DPYD)	ENSP00000359211.3:p.Val765Met
NM_000110.3:c.2293G>A , LRG_722t1:c.2293G>A (DPYD)	NP_000101.2:p.Val765Met
NR_046590.1:n.129-924C>T (DPYD-AS1)
XM_005270562.3:c.2077G>A (DPYD)	XP_005270619.2:p.Val693Met
XM_006710397.2:c.2293G>A (DPYD)	XP_006710460.1:p.Val765Met
XM_006710397.3:c.2293G>A (DPYD)	XP_006710460.1:p.Val765Met
XM_017000507.1:c.2182G>A (DPYD)	XP_016855996.1:p.Val728Met
XM_017000508.2:c.1798G>A (DPYD)	XP_016855997.1:p.Val600Met
XM_017000509.2:c.1798G>A (DPYD)	XP_016855998.1:p.Val600Met
XM_017000510.1:c.1798G>A (DPYD)	XP_016855999.1:p.Val600Met
NM_000110.4:c.2293G>A (DPYD) MANE Select	NP_000101.2:p.Val765Met