Canonical Allele Identifier: CA1452058572
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277108G= , CM000666.2:g.39277108G= GRCh38
NC_000004.11:g.39278728G= , CM000666.1:g.39278728G= GRCh37
NC_000004.10:g.38955123G= NCBI36
NG_031813.1:g.99705G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3805G= MANE Select ENSP00000382717.3:p.Gly1269=
ENST00000399820.7:c.3805G= ENSP00000382717.3:p.Gly1269=
ENST00000503733.1:n.145G=
ENST00000506869.5:c.*3386G= ENSP00000424319.1:n.*3386G=
ENST00000512534.5:n.2116G=
ENST00000512588.5:n.147G=
NM_025132.3:c.3805G= NP_079408.3:p.Gly1269=
XM_011513724.1:c.3817G= XP_011512026.1:p.Gly1273=
XM_011513725.1:c.3751G= XP_011512027.1:p.Gly1251=
XM_011513726.1:c.3337G= XP_011512028.1:p.Gly1113=
XM_011513727.1:c.3337G= XP_011512029.1:p.Gly1113=
XM_011513728.1:c.3325G= XP_011512030.1:p.Gly1109=
XR_925155.1:n.5515G=
NM_001317924.1:c.3325G= NP_001304853.1:p.Gly1109=
XM_011513725.2:c.3751G= XP_011512027.1:p.Gly1251=
XM_011513726.3:c.3337G= XP_011512028.1:p.Gly1113=
XM_017008501.1:c.3325G= XP_016863990.1:p.Gly1109=
XR_001741306.1:n.4082G=
XR_001741307.1:n.4070G=
XR_001741308.1:n.5716G=
XR_001741309.1:n.5503G=
XR_001741310.1:n.5704G=
XR_001741311.2:n.5352G=
NM_025132.4:c.3805G= MANE Select NP_079408.3:p.Gly1269=
NM_001317924.2:c.3325G= NP_001304853.1:p.Gly1109=