Canonical Allele Identifier: CA419137745

Gene: DPYD DPYD-AS1

Linked Data

• MyVariant Identifiers: chr1:g.97700423A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97234867A>C , CM000663.2:g.97234867A>C	GRCh38
NC_000001.10:g.97700423A>C , CM000663.1:g.97700423A>C	GRCh37
NC_000001.9:g.97473011A>C	NCBI36
NG_008807.2:g.691193T>G , LRG_722:g.691193T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2427T>G (DPYD) MANE Select	ENSP00000359211.3:p.Gly809=
ENST00000370192.7:c.2427T>G (DPYD)	ENSP00000359211.3:p.Gly809=
NM_000110.3:c.2427T>G , LRG_722t1:c.2427T>G (DPYD)	NP_000101.2:p.Gly809=
NR_046590.1:n.65-30547A>C (DPYD-AS1)
XM_005270562.3:c.2211T>G (DPYD)	XP_005270619.2:p.Gly737=
XM_006710397.2:c.2427T>G (DPYD)	XP_006710460.1:p.Gly809=
XM_006710397.3:c.2427T>G (DPYD)	XP_006710460.1:p.Gly809=
XM_017000507.1:c.2316T>G (DPYD)	XP_016855996.1:p.Gly772=
XM_017000508.2:c.1932T>G (DPYD)	XP_016855997.1:p.Gly644=
XM_017000509.2:c.1932T>G (DPYD)	XP_016855998.1:p.Gly644=
XM_017000510.1:c.1932T>G (DPYD)	XP_016855999.1:p.Gly644=
NM_000110.4:c.2427T>G (DPYD) MANE Select	NP_000101.2:p.Gly809=