Canonical Allele Identifier: CA341374555

Gene: DPYD DPYD-AS1

Linked Data

• ClinVar Variation Id: 976091
• ClinVar RCV Id: RCV001253275
• dbSNP Id: rs777673186
• MyVariant Identifiers: chr1:g.97700493G>T (hg19) ; chr1:g.97234937G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234937G>T , CM000663.2:g.97234937G>T	GRCh38
NC_000001.10:g.97700493G>T , CM000663.1:g.97700493G>T	GRCh37
NC_000001.9:g.97473081G>T	NCBI36
NG_008807.2:g.691123C>A , LRG_722:g.691123C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2357C>A (DPYD) MANE Select	ENSP00000359211.3:p.Pro786His
ENST00000370192.7:c.2357C>A (DPYD)	ENSP00000359211.3:p.Pro786His
NM_000110.3:c.2357C>A , LRG_722t1:c.2357C>A (DPYD)	NP_000101.2:p.Pro786His
NR_046590.1:n.65-30477G>T (DPYD-AS1)
XM_005270562.3:c.2141C>A (DPYD)	XP_005270619.2:p.Pro714His
XM_006710397.2:c.2357C>A (DPYD)	XP_006710460.1:p.Pro786His
XM_006710397.3:c.2357C>A (DPYD)	XP_006710460.1:p.Pro786His
XM_017000507.1:c.2246C>A (DPYD)	XP_016855996.1:p.Pro749His
XM_017000508.2:c.1862C>A (DPYD)	XP_016855997.1:p.Pro621His
XM_017000509.2:c.1862C>A (DPYD)	XP_016855998.1:p.Pro621His
XM_017000510.1:c.1862C>A (DPYD)	XP_016855999.1:p.Pro621His
NM_000110.4:c.2357C>A (DPYD) MANE Select	NP_000101.2:p.Pro786His