Canonical Allele Identifier: CA1452058574
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277111T= , CM000666.2:g.39277111T= GRCh38
NC_000004.11:g.39278731T= , CM000666.1:g.39278731T= GRCh37
NC_000004.10:g.38955126T= NCBI36
NG_031813.1:g.99708T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3808T= MANE Select ENSP00000382717.3:p.Cys1270=
ENST00000399820.7:c.3808T= ENSP00000382717.3:p.Cys1270=
ENST00000503733.1:n.148T=
ENST00000506869.5:c.*3389T= ENSP00000424319.1:n.*3389T=
ENST00000512534.5:n.2119T=
ENST00000512588.5:n.150T=
NM_025132.3:c.3808T= NP_079408.3:p.Cys1270=
XM_011513724.1:c.3820T= XP_011512026.1:p.Cys1274=
XM_011513725.1:c.3754T= XP_011512027.1:p.Cys1252=
XM_011513726.1:c.3340T= XP_011512028.1:p.Cys1114=
XM_011513727.1:c.3340T= XP_011512029.1:p.Cys1114=
XM_011513728.1:c.3328T= XP_011512030.1:p.Cys1110=
XR_925155.1:n.5518T=
NM_001317924.1:c.3328T= NP_001304853.1:p.Cys1110=
XM_011513725.2:c.3754T= XP_011512027.1:p.Cys1252=
XM_011513726.3:c.3340T= XP_011512028.1:p.Cys1114=
XM_017008501.1:c.3328T= XP_016863990.1:p.Cys1110=
XR_001741306.1:n.4085T=
XR_001741307.1:n.4073T=
XR_001741308.1:n.5719T=
XR_001741309.1:n.5506T=
XR_001741310.1:n.5707T=
XR_001741311.2:n.5355T=
NM_025132.4:c.3808T= MANE Select NP_079408.3:p.Cys1270=
NM_001317924.2:c.3328T= NP_001304853.1:p.Cys1110=