Canonical Allele Identifier: CA1452058555
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39277103G= , CM000666.2:g.39277103G= GRCh38
NC_000004.11:g.39278723G= , CM000666.1:g.39278723G= GRCh37
NC_000004.10:g.38955118G= NCBI36
NG_031813.1:g.99700G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3800G= MANE Select ENSP00000382717.3:p.Cys1267=
ENST00000399820.7:c.3800G= ENSP00000382717.3:p.Cys1267=
ENST00000503733.1:n.140G=
ENST00000506869.5:c.*3381G= ENSP00000424319.1:n.*3381G=
ENST00000512534.5:n.2111G=
ENST00000512588.5:n.142G=
NM_025132.3:c.3800G= NP_079408.3:p.Cys1267=
XM_011513724.1:c.3812G= XP_011512026.1:p.Cys1271=
XM_011513725.1:c.3746G= XP_011512027.1:p.Cys1249=
XM_011513726.1:c.3332G= XP_011512028.1:p.Cys1111=
XM_011513727.1:c.3332G= XP_011512029.1:p.Cys1111=
XM_011513728.1:c.3320G= XP_011512030.1:p.Cys1107=
XR_925155.1:n.5510G=
NM_001317924.1:c.3320G= NP_001304853.1:p.Cys1107=
XM_011513725.2:c.3746G= XP_011512027.1:p.Cys1249=
XM_011513726.3:c.3332G= XP_011512028.1:p.Cys1111=
XM_017008501.1:c.3320G= XP_016863990.1:p.Cys1107=
XR_001741306.1:n.4077G=
XR_001741307.1:n.4065G=
XR_001741308.1:n.5711G=
XR_001741309.1:n.5498G=
XR_001741310.1:n.5699G=
XR_001741311.2:n.5347G=
NM_025132.4:c.3800G= MANE Select NP_079408.3:p.Cys1267=
NM_001317924.2:c.3320G= NP_001304853.1:p.Cys1107=