Canonical Allele Identifier: CA1452055210
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39273042C= , CM000666.2:g.39273042C= GRCh38
NC_000004.11:g.39274662C= , CM000666.1:g.39274662C= GRCh37
NC_000004.10:g.38951057C= NCBI36
NG_031813.1:g.95639C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3546C= MANE Select ENSP00000382717.3:p.Asn1182=
ENST00000399820.7:c.3546C= ENSP00000382717.3:p.Asn1182=
ENST00000506869.5:c.*3127C= ENSP00000424319.1:n.*3127C=
ENST00000512095.5:n.2544C=
ENST00000512534.5:n.111C=
NM_025132.3:c.3546C= NP_079408.3:p.Asn1182=
XM_011513724.1:c.3558C= XP_011512026.1:p.Asn1186=
XM_011513725.1:c.3492C= XP_011512027.1:p.Asn1164=
XM_011513726.1:c.3078C= XP_011512028.1:p.Asn1026=
XM_011513727.1:c.3078C= XP_011512029.1:p.Asn1026=
XM_011513728.1:c.3066C= XP_011512030.1:p.Asn1022=
XR_925155.1:n.3622C=
NM_001317924.1:c.3066C= NP_001304853.1:p.Asn1022=
XM_011513725.2:c.3492C= XP_011512027.1:p.Asn1164=
XM_011513726.3:c.3078C= XP_011512028.1:p.Asn1026=
XM_017008501.1:c.3066C= XP_016863990.1:p.Asn1022=
XR_001741306.1:n.3622C=
XR_001741307.1:n.3610C=
XR_001741308.1:n.3622C=
XR_001741309.1:n.3610C=
XR_001741310.1:n.3610C=
XR_001741311.2:n.3459C=
NM_025132.4:c.3546C= MANE Select NP_079408.3:p.Asn1182=
NM_001317924.2:c.3066C= NP_001304853.1:p.Asn1022=