Canonical Allele Identifier: CA550723000
Gene: WDR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205194del , CM000666.2:g.39205194del GRCh38
NC_000004.11:g.39206814del , CM000666.1:g.39206814del GRCh37
NC_000004.10:g.38883209del NCBI36
NG_031813.1:g.27791del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.644del MANE Select ENSP00000382717.3:p.Asn215IlefsTer2
ENST00000399820.7:c.644del ENSP00000382717.3:p.Asn215IlefsTer2
ENST00000503697.5:c.*112del ENSP00000423706.1:n.*112del
ENST00000505055.5:c.*225del ENSP00000425949.1:n.*225del
ENST00000506503.1:c.644del ENSP00000423491.1:p.Asn215IlefsTer2
ENST00000506869.5:c.*225del ENSP00000424319.1:n.*225del
ENST00000511729.5:n.40+22631del
ENST00000512448.1:n.238del
NM_025132.3:c.644del NP_079408.3:p.Asn215IlefsTer2
XM_011513724.1:c.644del XP_011512026.1:p.Asn215IlefsTer2
XM_011513725.1:c.578del XP_011512027.1:p.Asn193IlefsTer2
XM_011513726.1:c.164del XP_011512028.1:p.Asn55IlefsTer2
XM_011513727.1:c.164del XP_011512029.1:p.Asn55IlefsTer2
XM_011513728.1:c.164del XP_011512030.1:p.Asn55IlefsTer2
XM_011513729.1:c.644del XP_011512031.1:p.Asn215IlefsTer2
XR_925155.1:n.708del
NM_001317924.1:c.164del NP_001304853.1:p.Asn55IlefsTer2
XM_011513725.2:c.578del XP_011512027.1:p.Asn193IlefsTer2
XM_011513726.3:c.164del XP_011512028.1:p.Asn55IlefsTer2
XM_017008501.1:c.164del XP_016863990.1:p.Asn55IlefsTer2
XR_001741306.1:n.708del
XR_001741307.1:n.708del
XR_001741308.1:n.708del
XR_001741309.1:n.708del
XR_001741310.1:n.708del
XR_001741311.2:n.557del
XR_001741312.1:n.708del
NM_025132.4:c.644del MANE Select NP_079408.3:p.Asn215IlefsTer2
NM_001317924.2:c.164del NP_001304853.1:p.Asn55IlefsTer2