Canonical Allele Identifier: CA1452058564
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277104T= , CM000666.2:g.39277104T= GRCh38
NC_000004.11:g.39278724T= , CM000666.1:g.39278724T= GRCh37
NC_000004.10:g.38955119T= NCBI36
NG_031813.1:g.99701T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3801T= MANE Select ENSP00000382717.3:p.Cys1267=
ENST00000399820.7:c.3801T= ENSP00000382717.3:p.Cys1267=
ENST00000503733.1:n.141T=
ENST00000506869.5:c.*3382T= ENSP00000424319.1:n.*3382T=
ENST00000512534.5:n.2112T=
ENST00000512588.5:n.143T=
NM_025132.3:c.3801T= NP_079408.3:p.Cys1267=
XM_011513724.1:c.3813T= XP_011512026.1:p.Cys1271=
XM_011513725.1:c.3747T= XP_011512027.1:p.Cys1249=
XM_011513726.1:c.3333T= XP_011512028.1:p.Cys1111=
XM_011513727.1:c.3333T= XP_011512029.1:p.Cys1111=
XM_011513728.1:c.3321T= XP_011512030.1:p.Cys1107=
XR_925155.1:n.5511T=
NM_001317924.1:c.3321T= NP_001304853.1:p.Cys1107=
XM_011513725.2:c.3747T= XP_011512027.1:p.Cys1249=
XM_011513726.3:c.3333T= XP_011512028.1:p.Cys1111=
XM_017008501.1:c.3321T= XP_016863990.1:p.Cys1107=
XR_001741306.1:n.4078T=
XR_001741307.1:n.4066T=
XR_001741308.1:n.5712T=
XR_001741309.1:n.5499T=
XR_001741310.1:n.5700T=
XR_001741311.2:n.5348T=
NM_025132.4:c.3801T= MANE Select NP_079408.3:p.Cys1267=
NM_001317924.2:c.3321T= NP_001304853.1:p.Cys1107=