Canonical Allele Identifier: CA1452058567
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277106C= , CM000666.2:g.39277106C= GRCh38
NC_000004.11:g.39278726C= , CM000666.1:g.39278726C= GRCh37
NC_000004.10:g.38955121C= NCBI36
NG_031813.1:g.99703C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3803C= MANE Select ENSP00000382717.3:p.Pro1268=
ENST00000399820.7:c.3803C= ENSP00000382717.3:p.Pro1268=
ENST00000503733.1:n.143C=
ENST00000506869.5:c.*3384C= ENSP00000424319.1:n.*3384C=
ENST00000512534.5:n.2114C=
ENST00000512588.5:n.145C=
NM_025132.3:c.3803C= NP_079408.3:p.Pro1268=
XM_011513724.1:c.3815C= XP_011512026.1:p.Pro1272=
XM_011513725.1:c.3749C= XP_011512027.1:p.Pro1250=
XM_011513726.1:c.3335C= XP_011512028.1:p.Pro1112=
XM_011513727.1:c.3335C= XP_011512029.1:p.Pro1112=
XM_011513728.1:c.3323C= XP_011512030.1:p.Pro1108=
XR_925155.1:n.5513C=
NM_001317924.1:c.3323C= NP_001304853.1:p.Pro1108=
XM_011513725.2:c.3749C= XP_011512027.1:p.Pro1250=
XM_011513726.3:c.3335C= XP_011512028.1:p.Pro1112=
XM_017008501.1:c.3323C= XP_016863990.1:p.Pro1108=
XR_001741306.1:n.4080C=
XR_001741307.1:n.4068C=
XR_001741308.1:n.5714C=
XR_001741309.1:n.5501C=
XR_001741310.1:n.5702C=
XR_001741311.2:n.5350C=
NM_025132.4:c.3803C= MANE Select NP_079408.3:p.Pro1268=
NM_001317924.2:c.3323C= NP_001304853.1:p.Pro1108=