Canonical Allele Identifier: CA1452063293

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244481A= , CM000666.2:g.39244481A=	GRCh38
NC_000004.11:g.39246101A= , CM000666.1:g.39246101A=	GRCh37
NC_000004.10:g.38922496A=	NCBI36
NG_031813.1:g.67078A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2574A= MANE Select	ENSP00000382717.3:p.Glu858=
ENST00000399820.7:c.2574A=	ENSP00000382717.3:p.Glu858=
ENST00000506869.5:c.*2155A=	ENSP00000424319.1:n.*2155A=
ENST00000512095.5:n.1572A=
NM_025132.3:c.2574A=	NP_079408.3:p.Glu858=
XM_011513724.1:c.2586A=	XP_011512026.1:p.Glu862=
XM_011513725.1:c.2520A=	XP_011512027.1:p.Glu840=
XM_011513726.1:c.2106A=	XP_011512028.1:p.Glu702=
XM_011513727.1:c.2106A=	XP_011512029.1:p.Glu702=
XM_011513728.1:c.2094A=	XP_011512030.1:p.Glu698=
XM_011513729.1:c.2586A=	XP_011512031.1:p.Glu862=
XR_925155.1:n.2650A=
NM_001317924.1:c.2094A=	NP_001304853.1:p.Glu698=
XM_011513725.2:c.2520A=	XP_011512027.1:p.Glu840=
XM_011513726.3:c.2106A=	XP_011512028.1:p.Glu702=
XM_017008501.1:c.2094A=	XP_016863990.1:p.Glu698=
XR_001741306.1:n.2650A=
XR_001741307.1:n.2638A=
XR_001741308.1:n.2650A=
XR_001741309.1:n.2638A=
XR_001741310.1:n.2638A=
XR_001741311.2:n.2487A=
NM_025132.4:c.2574A= MANE Select	NP_079408.3:p.Glu858=
NM_001317924.2:c.2094A=	NP_001304853.1:p.Glu698=