Canonical Allele Identifier: CA341377756

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.98015222T>C (hg19) ; chr1:g.97549666T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549666T>C , CM000663.2:g.97549666T>C	GRCh38
NC_000001.10:g.98015222T>C , CM000663.1:g.98015222T>C	GRCh37
NC_000001.9:g.97787810T>C	NCBI36
NG_008807.2:g.376394A>G , LRG_722:g.376394A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1418A>G MANE Select	ENSP00000359211.3:p.Glu473Gly
ENST00000370192.7:c.1418A>G	ENSP00000359211.3:p.Glu473Gly
NM_000110.3:c.1418A>G , LRG_722t1:c.1418A>G	NP_000101.2:p.Glu473Gly
XM_005270562.3:c.1418A>G	XP_005270619.2:p.Glu473Gly
XM_006710397.2:c.1418A>G	XP_006710460.1:p.Glu473Gly
XM_006710397.3:c.1418A>G	XP_006710460.1:p.Glu473Gly
XM_017000507.1:c.1307A>G	XP_016855996.1:p.Glu436Gly
XM_017000508.2:c.923A>G	XP_016855997.1:p.Glu308Gly
XM_017000509.2:c.923A>G	XP_016855998.1:p.Glu308Gly
XM_017000510.1:c.923A>G	XP_016855999.1:p.Glu308Gly
NM_000110.4:c.1418A>G MANE Select	NP_000101.2:p.Glu473Gly