Canonical Allele Identifier: CA962974

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs762911226
• ExAC: 1:97564179 T / A
• gnomAD v2: 1-97564179-T-A
• gnomAD v4: 1-97098623-T-A
• MyVariant Identifiers: chr1:g.97564179T>A (hg19) ; chr1:g.97098623T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2632A>T (DPYD) MANE Select	ENSP00000359211.3:p.Ser878Cys
ENST00000370192.7:c.2632A>T (DPYD)	ENSP00000359211.3:p.Ser878Cys
NM_000110.3:c.2632A>T , LRG_722t1:c.2632A>T (DPYD)	NP_000101.2:p.Ser878Cys
NR_046590.1:n.64+2637T>A (DPYD-AS1)
XM_005270562.3:c.2416A>T (DPYD)	XP_005270619.2:p.Ser806Cys
XM_017000507.1:c.2521A>T (DPYD)	XP_016855996.1:p.Ser841Cys
XM_017000508.2:c.2137A>T (DPYD)	XP_016855997.1:p.Ser713Cys
XM_017000509.2:c.2137A>T (DPYD)	XP_016855998.1:p.Ser713Cys
XM_017000510.1:c.2137A>T (DPYD)	XP_016855999.1:p.Ser713Cys
NM_000110.4:c.2632A>T (DPYD) MANE Select	NP_000101.2:p.Ser878Cys