Canonical Allele Identifier: CA963089

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs60511679
• ExAC: 1:97770919 A / C
• gnomAD v2: 1-97770919-A-C
• gnomAD v3: 1-97305363-A-C
• gnomAD v4: 1-97305363-A-C
• MyVariant Identifiers: chr1:g.97770919A>C (hg19) ; chr1:g.97305363A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305363A>C , CM000663.2:g.97305363A>C	GRCh38
NC_000001.10:g.97770919A>C , CM000663.1:g.97770919A>C	GRCh37
NC_000001.9:g.97543507A>C	NCBI36
NG_008807.2:g.620697T>G , LRG_722:g.620697T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2195T>G (DPYD) MANE Select	ENSP00000359211.3:p.Val732Gly
ENST00000370192.7:c.2195T>G (DPYD)	ENSP00000359211.3:p.Val732Gly
NM_000110.3:c.2195T>G , LRG_722t1:c.2195T>G (DPYD)	NP_000101.2:p.Val732Gly
NR_046590.1:n.129-826A>C (DPYD-AS1)
XM_005270562.3:c.1979T>G (DPYD)	XP_005270619.2:p.Val660Gly
XM_006710397.2:c.2195T>G (DPYD)	XP_006710460.1:p.Val732Gly
XM_006710397.3:c.2195T>G (DPYD)	XP_006710460.1:p.Val732Gly
XM_017000507.1:c.2084T>G (DPYD)	XP_016855996.1:p.Val695Gly
XM_017000508.2:c.1700T>G (DPYD)	XP_016855997.1:p.Val567Gly
XM_017000509.2:c.1700T>G (DPYD)	XP_016855998.1:p.Val567Gly
XM_017000510.1:c.1700T>G (DPYD)	XP_016855999.1:p.Val567Gly
NM_000110.4:c.2195T>G (DPYD) MANE Select	NP_000101.2:p.Val732Gly