Canonical Allele Identifier: CA1452055205
Gene: WDR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39273039C= , CM000666.2:g.39273039C= GRCh38
NC_000004.11:g.39274659C= , CM000666.1:g.39274659C= GRCh37
NC_000004.10:g.38951054C= NCBI36
NG_031813.1:g.95636C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.3543C= MANE Select ENSP00000382717.3:p.Asn1181=
ENST00000399820.7:c.3543C= ENSP00000382717.3:p.Asn1181=
ENST00000506869.5:c.*3124C= ENSP00000424319.1:n.*3124C=
ENST00000512095.5:n.2541C=
ENST00000512534.5:n.108C=
NM_025132.3:c.3543C= NP_079408.3:p.Asn1181=
XM_011513724.1:c.3555C= XP_011512026.1:p.Asn1185=
XM_011513725.1:c.3489C= XP_011512027.1:p.Asn1163=
XM_011513726.1:c.3075C= XP_011512028.1:p.Asn1025=
XM_011513727.1:c.3075C= XP_011512029.1:p.Asn1025=
XM_011513728.1:c.3063C= XP_011512030.1:p.Asn1021=
XR_925155.1:n.3619C=
NM_001317924.1:c.3063C= NP_001304853.1:p.Asn1021=
XM_011513725.2:c.3489C= XP_011512027.1:p.Asn1163=
XM_011513726.3:c.3075C= XP_011512028.1:p.Asn1025=
XM_017008501.1:c.3063C= XP_016863990.1:p.Asn1021=
XR_001741306.1:n.3619C=
XR_001741307.1:n.3607C=
XR_001741308.1:n.3619C=
XR_001741309.1:n.3607C=
XR_001741310.1:n.3607C=
XR_001741311.2:n.3456C=
NM_025132.4:c.3543C= MANE Select NP_079408.3:p.Asn1181=
NM_001317924.2:c.3063C= NP_001304853.1:p.Asn1021=