Canonical Allele Identifier: CA2646705131

Gene: DPYD

Linked Data

• gnomAD v4: 1-97382305-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382305G>A , CM000663.2:g.97382305G>A	GRCh38
NC_000001.10:g.97847861G>A , CM000663.1:g.97847861G>A	GRCh37
NC_000001.9:g.97620449G>A	NCBI36
NG_008807.2:g.543755C>T , LRG_722:g.543755C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1974+88C>T MANE Select	ENSP00000359211.3:n.1974+88C>T
ENST00000370192.7:c.1974+88C>T	ENSP00000359211.3:n.1974+88C>T
NM_000110.3:c.1974+88C>T , LRG_722t1:c.1974+88C>T	NP_000101.2:n.1974+88C>T
XM_005270562.3:c.1758+88C>T	XP_005270619.2:n.1758+88C>T
XM_006710397.2:c.1974+88C>T	XP_006710460.1:n.1974+88C>T
XR_947619.1:n.1347-1329G>A
XR_947620.1:n.1125-1329G>A
XR_947621.1:n.1347-1329G>A
XM_006710397.3:c.1974+88C>T	XP_006710460.1:n.1974+88C>T
XM_017000507.1:c.1863+88C>T	XP_016855996.1:n.1863+88C>T
XM_017000508.2:c.1479+88C>T	XP_016855997.1:n.1479+88C>T
XM_017000509.2:c.1479+88C>T	XP_016855998.1:n.1479+88C>T
XM_017000510.1:c.1479+88C>T	XP_016855999.1:n.1479+88C>T
XR_001737686.2:n.692-1329G>A
XR_001737687.1:n.692-1329G>A
XR_001737688.2:n.692-1329G>A
NM_000110.4:c.1974+88C>T MANE Select	NP_000101.2:n.1974+88C>T