Canonical Allele Identifier: CA963181

Gene: DPYD

Linked Data

• dbSNP Id: rs766786116
• ExAC: 1:97847919 AAAAT / A
• gnomAD v2: 1-97847919-AAAAT-A
• gnomAD v4: 1-97382363-AAAAT-A
• MyVariant Identifiers: chr1:g.97847920_97847923del (hg19) ; chr1:g.97382364_97382367del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382369_97382372del , CM000663.2:g.97382369_97382372del	GRCh38
NC_000001.10:g.97847925_97847928del , CM000663.1:g.97847925_97847928del	GRCh37
NC_000001.9:g.97620513_97620516del	NCBI36
NG_008807.2:g.543693_543696del , LRG_722:g.543693_543696del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1974+26_1974+29del MANE Select	ENSP00000359211.3:n.1974+26_1974+29del
ENST00000370192.7:c.1974+26_1974+29del	ENSP00000359211.3:n.1974+26_1974+29del
NM_000110.3:c.1974+26_1974+29del , LRG_722t1:c.1974+26_1974+29del	NP_000101.2:n.1974+26_1974+29del
XM_005270562.3:c.1758+26_1758+29del	XP_005270619.2:n.1758+26_1758+29del
XM_006710397.2:c.1974+26_1974+29del	XP_006710460.1:n.1974+26_1974+29del
XR_947619.1:n.1347-1265_1347-1262del
XR_947620.1:n.1125-1265_1125-1262del
XR_947621.1:n.1347-1265_1347-1262del
XM_006710397.3:c.1974+26_1974+29del	XP_006710460.1:n.1974+26_1974+29del
XM_017000507.1:c.1863+26_1863+29del	XP_016855996.1:n.1863+26_1863+29del
XM_017000508.2:c.1479+26_1479+29del	XP_016855997.1:n.1479+26_1479+29del
XM_017000509.2:c.1479+26_1479+29del	XP_016855998.1:n.1479+26_1479+29del
XM_017000510.1:c.1479+26_1479+29del	XP_016855999.1:n.1479+26_1479+29del
XR_001737686.2:n.692-1265_692-1262del
XR_001737687.1:n.692-1265_692-1262del
XR_001737688.2:n.692-1265_692-1262del
NM_000110.4:c.1974+26_1974+29del MANE Select	NP_000101.2:n.1974+26_1974+29del