Canonical Allele Identifier: CA1452058569
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277107T= , CM000666.2:g.39277107T= GRCh38
NC_000004.11:g.39278727T= , CM000666.1:g.39278727T= GRCh37
NC_000004.10:g.38955122T= NCBI36
NG_031813.1:g.99704T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3804T= MANE Select ENSP00000382717.3:p.Pro1268=
ENST00000399820.7:c.3804T= ENSP00000382717.3:p.Pro1268=
ENST00000503733.1:n.144T=
ENST00000506869.5:c.*3385T= ENSP00000424319.1:n.*3385T=
ENST00000512534.5:n.2115T=
ENST00000512588.5:n.146T=
NM_025132.3:c.3804T= NP_079408.3:p.Pro1268=
XM_011513724.1:c.3816T= XP_011512026.1:p.Pro1272=
XM_011513725.1:c.3750T= XP_011512027.1:p.Pro1250=
XM_011513726.1:c.3336T= XP_011512028.1:p.Pro1112=
XM_011513727.1:c.3336T= XP_011512029.1:p.Pro1112=
XM_011513728.1:c.3324T= XP_011512030.1:p.Pro1108=
XR_925155.1:n.5514T=
NM_001317924.1:c.3324T= NP_001304853.1:p.Pro1108=
XM_011513725.2:c.3750T= XP_011512027.1:p.Pro1250=
XM_011513726.3:c.3336T= XP_011512028.1:p.Pro1112=
XM_017008501.1:c.3324T= XP_016863990.1:p.Pro1108=
XR_001741306.1:n.4081T=
XR_001741307.1:n.4069T=
XR_001741308.1:n.5715T=
XR_001741309.1:n.5502T=
XR_001741310.1:n.5703T=
XR_001741311.2:n.5351T=
NM_025132.4:c.3804T= MANE Select NP_079408.3:p.Pro1268=
NM_001317924.2:c.3324T= NP_001304853.1:p.Pro1108=