Canonical Allele Identifier: CA341375754

Gene: DPYD

Linked Data

• gnomAD v4: 1-97382406-G-T
• MyVariant Identifiers: chr1:g.97847962G>T (hg19) ; chr1:g.97382406G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382406G>T , CM000663.2:g.97382406G>T	GRCh38
NC_000001.10:g.97847962G>T , CM000663.1:g.97847962G>T	GRCh37
NC_000001.9:g.97620550G>T	NCBI36
NG_008807.2:g.543654C>A , LRG_722:g.543654C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1961C>A MANE Select	ENSP00000359211.3:p.Ala654Asp
ENST00000370192.7:c.1961C>A	ENSP00000359211.3:p.Ala654Asp
NM_000110.3:c.1961C>A , LRG_722t1:c.1961C>A	NP_000101.2:p.Ala654Asp
XM_005270562.3:c.1745C>A	XP_005270619.2:p.Ala582Asp
XM_006710397.2:c.1961C>A	XP_006710460.1:p.Ala654Asp
XR_947619.1:n.1347-1228G>T
XR_947620.1:n.1125-1228G>T
XR_947621.1:n.1347-1228G>T
XM_006710397.3:c.1961C>A	XP_006710460.1:p.Ala654Asp
XM_017000507.1:c.1850C>A	XP_016855996.1:p.Ala617Asp
XM_017000508.2:c.1466C>A	XP_016855997.1:p.Ala489Asp
XM_017000509.2:c.1466C>A	XP_016855998.1:p.Ala489Asp
XM_017000510.1:c.1466C>A	XP_016855999.1:p.Ala489Asp
XR_001737686.2:n.692-1228G>T
XR_001737687.1:n.692-1228G>T
XR_001737688.2:n.692-1228G>T
NM_000110.4:c.1961C>A MANE Select	NP_000101.2:p.Ala654Asp