Canonical Allele Identifier: CA341376012

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97915664G>T (hg19) ; chr1:g.97450108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450108G>T , CM000663.2:g.97450108G>T	GRCh38
NC_000001.10:g.97915664G>T , CM000663.1:g.97915664G>T	GRCh37
NC_000001.9:g.97688252G>T	NCBI36
NG_008807.2:g.475952C>A , LRG_722:g.475952C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1856C>A MANE Select	ENSP00000359211.3:p.Ala619Glu
ENST00000370192.7:c.1856C>A	ENSP00000359211.3:p.Ala619Glu
NM_000110.3:c.1856C>A , LRG_722t1:c.1856C>A	NP_000101.2:p.Ala619Glu
XM_005270562.3:c.1640C>A	XP_005270619.2:p.Ala547Glu
XM_006710397.2:c.1856C>A	XP_006710460.1:p.Ala619Glu
XM_006710397.3:c.1856C>A	XP_006710460.1:p.Ala619Glu
XM_017000507.1:c.1745C>A	XP_016855996.1:p.Ala582Glu
XM_017000508.2:c.1361C>A	XP_016855997.1:p.Ala454Glu
XM_017000509.2:c.1361C>A	XP_016855998.1:p.Ala454Glu
XM_017000510.1:c.1361C>A	XP_016855999.1:p.Ala454Glu
NM_000110.4:c.1856C>A MANE Select	NP_000101.2:p.Ala619Glu