Canonical Allele Identifier: CA1452055193
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39273032T= , CM000666.2:g.39273032T= GRCh38
NC_000004.11:g.39274652T= , CM000666.1:g.39274652T= GRCh37
NC_000004.10:g.38951047T= NCBI36
NG_031813.1:g.95629T=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3536T= MANE Select ENSP00000382717.3:p.Val1179=
ENST00000399820.7:c.3536T= ENSP00000382717.3:p.Val1179=
ENST00000506869.5:c.*3117T= ENSP00000424319.1:n.*3117T=
ENST00000512095.5:n.2534T=
ENST00000512534.5:n.101T=
NM_025132.3:c.3536T= NP_079408.3:p.Val1179=
XM_011513724.1:c.3548T= XP_011512026.1:p.Val1183=
XM_011513725.1:c.3482T= XP_011512027.1:p.Val1161=
XM_011513726.1:c.3068T= XP_011512028.1:p.Val1023=
XM_011513727.1:c.3068T= XP_011512029.1:p.Val1023=
XM_011513728.1:c.3056T= XP_011512030.1:p.Val1019=
XR_925155.1:n.3612T=
NM_001317924.1:c.3056T= NP_001304853.1:p.Val1019=
XM_011513725.2:c.3482T= XP_011512027.1:p.Val1161=
XM_011513726.3:c.3068T= XP_011512028.1:p.Val1023=
XM_017008501.1:c.3056T= XP_016863990.1:p.Val1019=
XR_001741306.1:n.3612T=
XR_001741307.1:n.3600T=
XR_001741308.1:n.3612T=
XR_001741309.1:n.3600T=
XR_001741310.1:n.3600T=
XR_001741311.2:n.3449T=
NM_025132.4:c.3536T= MANE Select NP_079408.3:p.Val1179=
NM_001317924.2:c.3056T= NP_001304853.1:p.Val1019=