Canonical Allele Identifier: CA2646705091
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97382262_97382263del , CM000663.2:g.97382262_97382263del GRCh38
NC_000001.10:g.97847818_97847819del , CM000663.1:g.97847818_97847819del GRCh37
NC_000001.9:g.97620406_97620407del NCBI36
NG_008807.2:g.543798_543799del , LRG_722:g.543798_543799del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1974+131_1974+132del MANE Select ENSP00000359211.3:n.1974+131_1974+132del
ENST00000370192.7:c.1974+131_1974+132del ENSP00000359211.3:n.1974+131_1974+132del
NM_000110.3:c.1974+131_1974+132del , LRG_722t1:c.1974+131_1974+132del NP_000101.2:n.1974+131_1974+132del
XM_005270562.3:c.1758+131_1758+132del XP_005270619.2:n.1758+131_1758+132del
XM_006710397.2:c.1974+131_1974+132del XP_006710460.1:n.1974+131_1974+132del
XR_947619.1:n.1347-1372_1347-1371del
XR_947620.1:n.1125-1372_1125-1371del
XR_947621.1:n.1347-1372_1347-1371del
XM_006710397.3:c.1974+131_1974+132del XP_006710460.1:n.1974+131_1974+132del
XM_017000507.1:c.1863+131_1863+132del XP_016855996.1:n.1863+131_1863+132del
XM_017000508.2:c.1479+131_1479+132del XP_016855997.1:n.1479+131_1479+132del
XM_017000509.2:c.1479+131_1479+132del XP_016855998.1:n.1479+131_1479+132del
XM_017000510.1:c.1479+131_1479+132del XP_016855999.1:n.1479+131_1479+132del
XR_001737686.2:n.692-1372_692-1371del
XR_001737687.1:n.692-1372_692-1371del
XR_001737688.2:n.692-1372_692-1371del
NM_000110.4:c.1974+131_1974+132del MANE Select NP_000101.2:n.1974+131_1974+132del