Canonical Allele Identifier: CA1452055115

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39272998G= , CM000666.2:g.39272998G=	GRCh38
NC_000004.11:g.39274618G= , CM000666.1:g.39274618G=	GRCh37
NC_000004.10:g.38951013G=	NCBI36
NG_031813.1:g.95595G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3502G= MANE Select	ENSP00000382717.3:p.Asp1168=
ENST00000399820.7:c.3502G=	ENSP00000382717.3:p.Asp1168=
ENST00000506869.5:c.*3083G=	ENSP00000424319.1:n.*3083G=
ENST00000512095.5:n.2500G=
ENST00000512534.5:n.67G=
NM_025132.3:c.3502G=	NP_079408.3:p.Asp1168=
XM_011513724.1:c.3514G=	XP_011512026.1:p.Asp1172=
XM_011513725.1:c.3448G=	XP_011512027.1:p.Asp1150=
XM_011513726.1:c.3034G=	XP_011512028.1:p.Asp1012=
XM_011513727.1:c.3034G=	XP_011512029.1:p.Asp1012=
XM_011513728.1:c.3022G=	XP_011512030.1:p.Asp1008=
XR_925155.1:n.3578G=
NM_001317924.1:c.3022G=	NP_001304853.1:p.Asp1008=
XM_011513725.2:c.3448G=	XP_011512027.1:p.Asp1150=
XM_011513726.3:c.3034G=	XP_011512028.1:p.Asp1012=
XM_017008501.1:c.3022G=	XP_016863990.1:p.Asp1008=
XR_001741306.1:n.3578G=
XR_001741307.1:n.3566G=
XR_001741308.1:n.3578G=
XR_001741309.1:n.3566G=
XR_001741310.1:n.3566G=
XR_001741311.2:n.3415G=
NM_025132.4:c.3502G= MANE Select	NP_079408.3:p.Asp1168=
NM_001317924.2:c.3022G=	NP_001304853.1:p.Asp1008=