Canonical Allele Identifier: CA2670363050
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277026del , CM000666.2:g.39277026del GRCh38
NC_000004.11:g.39278646del , CM000666.1:g.39278646del GRCh37
NC_000004.10:g.38955041del NCBI36
NG_031813.1:g.99623del

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3723del MANE Select ENSP00000382717.3:p.Asp1242IlefsTer5
ENST00000399820.7:c.3723del ENSP00000382717.3:p.Asp1242IlefsTer5
ENST00000503733.1:n.63del
ENST00000506869.5:c.*3304del ENSP00000424319.1:n.*3304del
ENST00000512534.5:n.2034del
ENST00000512588.5:n.65del
NM_025132.3:c.3723del NP_079408.3:p.Asp1242IlefsTer5
XM_011513724.1:c.3735del XP_011512026.1:p.Asp1246IlefsTer5
XM_011513725.1:c.3669del XP_011512027.1:p.Asp1224IlefsTer5
XM_011513726.1:c.3255del XP_011512028.1:p.Asp1086IlefsTer5
XM_011513727.1:c.3255del XP_011512029.1:p.Asp1086IlefsTer5
XM_011513728.1:c.3243del XP_011512030.1:p.Asp1082IlefsTer5
XR_925155.1:n.5433del
NM_001317924.1:c.3243del NP_001304853.1:p.Asp1082IlefsTer5
XM_011513725.2:c.3669del XP_011512027.1:p.Asp1224IlefsTer5
XM_011513726.3:c.3255del XP_011512028.1:p.Asp1086IlefsTer5
XM_017008501.1:c.3243del XP_016863990.1:p.Asp1082IlefsTer5
XR_001741306.1:n.4000del
XR_001741307.1:n.3988del
XR_001741308.1:n.5634del
XR_001741309.1:n.5421del
XR_001741310.1:n.5622del
XR_001741311.2:n.5270del
NM_025132.4:c.3723del MANE Select NP_079408.3:p.Asp1242IlefsTer5
NM_001317924.2:c.3243del NP_001304853.1:p.Asp1082IlefsTer5