Canonical Allele Identifier: CA2646705266
Gene: DPYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97382532_97382538del , CM000663.2:g.97382532_97382538del GRCh38
NC_000001.10:g.97848088_97848094del , CM000663.1:g.97848088_97848094del GRCh37
NC_000001.9:g.97620676_97620682del NCBI36
NG_008807.2:g.543522_543528del , LRG_722:g.543522_543528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370192.8:c.1906-77_1906-71del MANE Select ENSP00000359211.3:n.1906-77_1906-71del
ENST00000370192.7:c.1906-77_1906-71del ENSP00000359211.3:n.1906-77_1906-71del
NM_000110.3:c.1906-77_1906-71del , LRG_722t1:c.1906-77_1906-71del NP_000101.2:n.1906-77_1906-71del
XM_005270562.3:c.1690-77_1690-71del XP_005270619.2:n.1690-77_1690-71del
XM_006710397.2:c.1906-77_1906-71del XP_006710460.1:n.1906-77_1906-71del
XR_947619.1:n.1347-1102_1347-1096del
XR_947620.1:n.1125-1102_1125-1096del
XR_947621.1:n.1347-1102_1347-1096del
XM_006710397.3:c.1906-77_1906-71del XP_006710460.1:n.1906-77_1906-71del
XM_017000507.1:c.1795-77_1795-71del XP_016855996.1:n.1795-77_1795-71del
XM_017000508.2:c.1411-77_1411-71del XP_016855997.1:n.1411-77_1411-71del
XM_017000509.2:c.1411-77_1411-71del XP_016855998.1:n.1411-77_1411-71del
XM_017000510.1:c.1411-77_1411-71del XP_016855999.1:n.1411-77_1411-71del
XR_001737686.2:n.692-1102_692-1096del
XR_001737687.1:n.692-1102_692-1096del
XR_001737688.2:n.692-1102_692-1096del
NM_000110.4:c.1906-77_1906-71del MANE Select NP_000101.2:n.1906-77_1906-71del