Canonical Allele Identifier: CA419137490

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101036802
• MyVariant Identifiers: chr1:g.97770927G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305371G>C , CM000663.2:g.97305371G>C	GRCh38
NC_000001.10:g.97770927G>C , CM000663.1:g.97770927G>C	GRCh37
NC_000001.9:g.97543515G>C	NCBI36
NG_008807.2:g.620689C>G , LRG_722:g.620689C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2187C>G (DPYD) MANE Select	ENSP00000359211.3:p.Ala729=
ENST00000370192.7:c.2187C>G (DPYD)	ENSP00000359211.3:p.Ala729=
NM_000110.3:c.2187C>G , LRG_722t1:c.2187C>G (DPYD)	NP_000101.2:p.Ala729=
NR_046590.1:n.129-818G>C (DPYD-AS1)
XM_005270562.3:c.1971C>G (DPYD)	XP_005270619.2:p.Ala657=
XM_006710397.2:c.2187C>G (DPYD)	XP_006710460.1:p.Ala729=
XM_006710397.3:c.2187C>G (DPYD)	XP_006710460.1:p.Ala729=
XM_017000507.1:c.2076C>G (DPYD)	XP_016855996.1:p.Ala692=
XM_017000508.2:c.1692C>G (DPYD)	XP_016855997.1:p.Ala564=
XM_017000509.2:c.1692C>G (DPYD)	XP_016855998.1:p.Ala564=
XM_017000510.1:c.1692C>G (DPYD)	XP_016855999.1:p.Ala564=
NM_000110.4:c.2187C>G (DPYD) MANE Select	NP_000101.2:p.Ala729=