Canonical Allele Identifier: CA10610856

Gene: DPYD DPYD-AS1

Linked Data

• ClinVar Variation Id: 298281
• ClinVar RCV Id: RCV000299078
• dbSNP Id: rs762911226
• MyVariant Identifiers: chr1:g.97564179T>C (hg19) ; chr1:g.97098623T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098623T>C , CM000663.2:g.97098623T>C	GRCh38
NC_000001.10:g.97564179T>C , CM000663.1:g.97564179T>C	GRCh37
NC_000001.9:g.97336767T>C	NCBI36
NG_008807.2:g.827437A>G , LRG_722:g.827437A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2632A>G (DPYD) MANE Select	ENSP00000359211.3:p.Ser878Gly
ENST00000370192.7:c.2632A>G (DPYD)	ENSP00000359211.3:p.Ser878Gly
NM_000110.3:c.2632A>G , LRG_722t1:c.2632A>G (DPYD)	NP_000101.2:p.Ser878Gly
NR_046590.1:n.64+2637T>C (DPYD-AS1)
XM_005270562.3:c.2416A>G (DPYD)	XP_005270619.2:p.Ser806Gly
XM_017000507.1:c.2521A>G (DPYD)	XP_016855996.1:p.Ser841Gly
XM_017000508.2:c.2137A>G (DPYD)	XP_016855997.1:p.Ser713Gly
XM_017000509.2:c.2137A>G (DPYD)	XP_016855998.1:p.Ser713Gly
XM_017000510.1:c.2137A>G (DPYD)	XP_016855999.1:p.Ser713Gly
NM_000110.4:c.2632A>G (DPYD) MANE Select	NP_000101.2:p.Ser878Gly