Canonical Allele Identifier: CA419140680

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97839147T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97373591T>C , CM000663.2:g.97373591T>C	GRCh38
NC_000001.10:g.97839147T>C , CM000663.1:g.97839147T>C	GRCh37
NC_000001.9:g.97611735T>C	NCBI36
NG_008807.2:g.552469A>G , LRG_722:g.552469A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2028A>G MANE Select	ENSP00000359211.3:p.Gly676=
ENST00000370192.7:c.2028A>G	ENSP00000359211.3:p.Gly676=
NM_000110.3:c.2028A>G , LRG_722t1:c.2028A>G	NP_000101.2:p.Gly676=
XM_005270562.3:c.1812A>G	XP_005270619.2:p.Gly604=
XM_006710397.2:c.2028A>G	XP_006710460.1:p.Gly676=
XR_947619.1:n.1125-1937T>C
XR_947620.1:n.1124+6390T>C
XR_947621.1:n.1125-1937T>C
XM_006710397.3:c.2028A>G	XP_006710460.1:p.Gly676=
XM_017000507.1:c.1917A>G	XP_016855996.1:p.Gly639=
XM_017000508.2:c.1533A>G	XP_016855997.1:p.Gly511=
XM_017000509.2:c.1533A>G	XP_016855998.1:p.Gly511=
XM_017000510.1:c.1533A>G	XP_016855999.1:p.Gly511=
NM_000110.4:c.2028A>G MANE Select	NP_000101.2:p.Gly676=