Canonical Allele Identifier: CA794675106
Gene: WDR19 HGNC NCBI

Linked Data

dbSNP Id: rs1193558900

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39275084_39275085del , CM000666.2:g.39275084_39275085del GRCh38
NC_000004.11:g.39276704_39276705del , CM000666.1:g.39276704_39276705del GRCh37
NC_000004.10:g.38953099_38953100del NCBI36
NG_031813.1:g.97681_97682del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.3716+126_3716+127del MANE Select ENSP00000382717.3:n.3716+126_3716+127del
ENST00000399820.7:c.3716+126_3716+127del ENSP00000382717.3:n.3716+126_3716+127del
ENST00000506869.5:c.*3297+126_*3297+127del ENSP00000424319.1:n.*3297+126_*3297+127del
ENST00000512095.5:n.2840_2841del
ENST00000512534.5:n.2027+126_2027+127del
NM_025132.3:c.3716+126_3716+127del NP_079408.3:n.3716+126_3716+127del
XM_011513724.1:c.3728+126_3728+127del XP_011512026.1:n.3728+126_3728+127del
XM_011513725.1:c.3662+126_3662+127del XP_011512027.1:n.3662+126_3662+127del
XM_011513726.1:c.3248+126_3248+127del XP_011512028.1:n.3248+126_3248+127del
XM_011513727.1:c.3248+126_3248+127del XP_011512029.1:n.3248+126_3248+127del
XM_011513728.1:c.3236+126_3236+127del XP_011512030.1:n.3236+126_3236+127del
XR_925155.1:n.5426+126_5426+127del
NM_001317924.1:c.3236+126_3236+127del NP_001304853.1:n.3236+126_3236+127del
XM_011513725.2:c.3662+126_3662+127del XP_011512027.1:n.3662+126_3662+127del
XM_011513726.3:c.3248+126_3248+127del XP_011512028.1:n.3248+126_3248+127del
XM_017008501.1:c.3236+126_3236+127del XP_016863990.1:n.3236+126_3236+127del
XR_001741306.1:n.3792+126_3792+127del
XR_001741307.1:n.3780+126_3780+127del
XR_001741308.1:n.5426+126_5426+127del
XR_001741309.1:n.5414+126_5414+127del
XR_001741310.1:n.5414+126_5414+127del
XR_001741311.2:n.5263+126_5263+127del
NM_025132.4:c.3716+126_3716+127del MANE Select NP_079408.3:n.3716+126_3716+127del
NM_001317924.2:c.3236+126_3236+127del NP_001304853.1:n.3236+126_3236+127del