Canonical Allele Identifier: CA1451995032
Gene: WDR19 HGNC NCBI

Linked Data

dbSNP Id: rs1727903319

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205901_39205902del , CM000666.2:g.39205901_39205902del GRCh38
NC_000004.11:g.39207521_39207522del , CM000666.1:g.39207521_39207522del GRCh37
NC_000004.10:g.38883916_38883917del NCBI36
NG_031813.1:g.28498_28499del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.890+165_890+166del MANE Select ENSP00000382717.3:n.890+165_890+166del
ENST00000399820.7:c.890+165_890+166del ENSP00000382717.3:n.890+165_890+166del
ENST00000503697.5:c.*358+165_*358+166del ENSP00000423706.1:n.*358+165_*358+166del
ENST00000506503.1:c.890+165_890+166del ENSP00000423491.1:n.890+165_890+166del
ENST00000506869.5:c.*471+165_*471+166del ENSP00000424319.1:n.*471+165_*471+166del
ENST00000511729.5:n.41-22657_41-22656del
ENST00000512448.1:n.649_650del
NM_025132.3:c.890+165_890+166del NP_079408.3:n.890+165_890+166del
XM_011513724.1:c.890+165_890+166del XP_011512026.1:n.890+165_890+166del
XM_011513725.1:c.824+165_824+166del XP_011512027.1:n.824+165_824+166del
XM_011513726.1:c.410+165_410+166del XP_011512028.1:n.410+165_410+166del
XM_011513727.1:c.410+165_410+166del XP_011512029.1:n.410+165_410+166del
XM_011513728.1:c.410+165_410+166del XP_011512030.1:n.410+165_410+166del
XM_011513729.1:c.890+165_890+166del XP_011512031.1:n.890+165_890+166del
XR_925155.1:n.954+165_954+166del
NM_001317924.1:c.410+165_410+166del NP_001304853.1:n.410+165_410+166del
XM_011513725.2:c.824+165_824+166del XP_011512027.1:n.824+165_824+166del
XM_011513726.3:c.410+165_410+166del XP_011512028.1:n.410+165_410+166del
XM_017008501.1:c.410+165_410+166del XP_016863990.1:n.410+165_410+166del
XR_001741306.1:n.954+165_954+166del
XR_001741307.1:n.954+165_954+166del
XR_001741308.1:n.954+165_954+166del
XR_001741309.1:n.954+165_954+166del
XR_001741310.1:n.954+165_954+166del
XR_001741311.2:n.803+165_803+166del
XR_001741312.1:n.954+165_954+166del
NM_025132.4:c.890+165_890+166del MANE Select NP_079408.3:n.890+165_890+166del
NM_001317924.2:c.410+165_410+166del NP_001304853.1:n.410+165_410+166del