Canonical Allele Identifier: CA341373395

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97193131-G-A
• MyVariant Identifiers: chr1:g.97658687G>A (hg19) ; chr1:g.97193131G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193131G>A , CM000663.2:g.97193131G>A	GRCh38
NC_000001.10:g.97658687G>A , CM000663.1:g.97658687G>A	GRCh37
NC_000001.9:g.97431275G>A	NCBI36
NG_008807.2:g.732929C>T , LRG_722:g.732929C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2560C>T (DPYD) MANE Select	ENSP00000359211.3:p.Pro854Ser
ENST00000370192.7:c.2560C>T (DPYD)	ENSP00000359211.3:p.Pro854Ser
NM_000110.3:c.2560C>T , LRG_722t1:c.2560C>T (DPYD)	NP_000101.2:p.Pro854Ser
NR_046590.1:n.65-72283G>A (DPYD-AS1)
XM_005270562.3:c.2344C>T (DPYD)	XP_005270619.2:p.Pro782Ser
XM_006710397.2:c.2560C>T (DPYD)	XP_006710460.1:p.Pro854Ser
XM_006710397.3:c.2560C>T (DPYD)	XP_006710460.1:p.Pro854Ser
XM_017000507.1:c.2449C>T (DPYD)	XP_016855996.1:p.Pro817Ser
XM_017000508.2:c.2065C>T (DPYD)	XP_016855997.1:p.Pro689Ser
XM_017000509.2:c.2065C>T (DPYD)	XP_016855998.1:p.Pro689Ser
XM_017000510.1:c.2065C>T (DPYD)	XP_016855999.1:p.Pro689Ser
NM_000110.4:c.2560C>T (DPYD) MANE Select	NP_000101.2:p.Pro854Ser