Canonical Allele Identifier: CA419145561
Gene: DPYD HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.97915681G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97450125G>T , CM000663.2:g.97450125G>T GRCh38
NC_000001.10:g.97915681G>T , CM000663.1:g.97915681G>T GRCh37
NC_000001.9:g.97688269G>T NCBI36
NG_008807.2:g.475935C>A , LRG_722:g.475935C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1839C>A MANE Select ENSP00000359211.3:p.Ile613=
ENST00000370192.7:c.1839C>A ENSP00000359211.3:p.Ile613=
NM_000110.3:c.1839C>A , LRG_722t1:c.1839C>A NP_000101.2:p.Ile613=
XM_005270562.3:c.1623C>A XP_005270619.2:p.Ile541=
XM_006710397.2:c.1839C>A XP_006710460.1:p.Ile613=
XM_006710397.3:c.1839C>A XP_006710460.1:p.Ile613=
XM_017000507.1:c.1728C>A XP_016855996.1:p.Ile576=
XM_017000508.2:c.1344C>A XP_016855997.1:p.Ile448=
XM_017000509.2:c.1344C>A XP_016855998.1:p.Ile448=
XM_017000510.1:c.1344C>A XP_016855999.1:p.Ile448=
NM_000110.4:c.1839C>A MANE Select NP_000101.2:p.Ile613=