Canonical Allele Identifier: CA95686457
Gene: WDR19 HGNC NCBI

Linked Data

dbSNP Id: rs1000813807

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205921_39205922del , CM000666.2:g.39205921_39205922del GRCh38
NC_000004.11:g.39207541_39207542del , CM000666.1:g.39207541_39207542del GRCh37
NC_000004.10:g.38883936_38883937del NCBI36
NG_031813.1:g.28518_28519del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.890+185_890+186del MANE Select ENSP00000382717.3:n.890+185_890+186del
ENST00000399820.7:c.890+185_890+186del ENSP00000382717.3:n.890+185_890+186del
ENST00000503697.5:c.*358+185_*358+186del ENSP00000423706.1:n.*358+185_*358+186del
ENST00000506503.1:c.890+185_890+186del ENSP00000423491.1:n.890+185_890+186del
ENST00000506869.5:c.*471+185_*471+186del ENSP00000424319.1:n.*471+185_*471+186del
ENST00000511729.5:n.41-22637_41-22636del
ENST00000512448.1:n.669_670del
NM_025132.3:c.890+185_890+186del NP_079408.3:n.890+185_890+186del
XM_011513724.1:c.890+185_890+186del XP_011512026.1:n.890+185_890+186del
XM_011513725.1:c.824+185_824+186del XP_011512027.1:n.824+185_824+186del
XM_011513726.1:c.410+185_410+186del XP_011512028.1:n.410+185_410+186del
XM_011513727.1:c.410+185_410+186del XP_011512029.1:n.410+185_410+186del
XM_011513728.1:c.410+185_410+186del XP_011512030.1:n.410+185_410+186del
XM_011513729.1:c.890+185_890+186del XP_011512031.1:n.890+185_890+186del
XR_925155.1:n.954+185_954+186del
NM_001317924.1:c.410+185_410+186del NP_001304853.1:n.410+185_410+186del
XM_011513725.2:c.824+185_824+186del XP_011512027.1:n.824+185_824+186del
XM_011513726.3:c.410+185_410+186del XP_011512028.1:n.410+185_410+186del
XM_017008501.1:c.410+185_410+186del XP_016863990.1:n.410+185_410+186del
XR_001741306.1:n.954+185_954+186del
XR_001741307.1:n.954+185_954+186del
XR_001741308.1:n.954+185_954+186del
XR_001741309.1:n.954+185_954+186del
XR_001741310.1:n.954+185_954+186del
XR_001741311.2:n.803+185_803+186del
XR_001741312.1:n.954+185_954+186del
NM_025132.4:c.890+185_890+186del MANE Select NP_079408.3:n.890+185_890+186del
NM_001317924.2:c.410+185_410+186del NP_001304853.1:n.410+185_410+186del