Canonical Allele Identifier: CA27484633

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs943095330
• gnomAD v4: 1-97305373-C-T
• COSMIC: COSM1345095
• MyVariant Identifiers: chr1:g.97770929C>T (hg19) ; chr1:g.97305373C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305373C>T , CM000663.2:g.97305373C>T	GRCh38
NC_000001.10:g.97770929C>T , CM000663.1:g.97770929C>T	GRCh37
NC_000001.9:g.97543517C>T	NCBI36
NG_008807.2:g.620687G>A , LRG_722:g.620687G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2185G>A (DPYD) MANE Select	ENSP00000359211.3:p.Ala729Thr
ENST00000370192.7:c.2185G>A (DPYD)	ENSP00000359211.3:p.Ala729Thr
NM_000110.3:c.2185G>A , LRG_722t1:c.2185G>A (DPYD)	NP_000101.2:p.Ala729Thr
NR_046590.1:n.129-816C>T (DPYD-AS1)
XM_005270562.3:c.1969G>A (DPYD)	XP_005270619.2:p.Ala657Thr
XM_006710397.2:c.2185G>A (DPYD)	XP_006710460.1:p.Ala729Thr
XM_006710397.3:c.2185G>A (DPYD)	XP_006710460.1:p.Ala729Thr
XM_017000507.1:c.2074G>A (DPYD)	XP_016855996.1:p.Ala692Thr
XM_017000508.2:c.1690G>A (DPYD)	XP_016855997.1:p.Ala564Thr
XM_017000509.2:c.1690G>A (DPYD)	XP_016855998.1:p.Ala564Thr
XM_017000510.1:c.1690G>A (DPYD)	XP_016855999.1:p.Ala564Thr
NM_000110.4:c.2185G>A (DPYD) MANE Select	NP_000101.2:p.Ala729Thr