Canonical Allele Identifier: CA1452063298

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244483C= , CM000666.2:g.39244483C=	GRCh38
NC_000004.11:g.39246103C= , CM000666.1:g.39246103C=	GRCh37
NC_000004.10:g.38922498C=	NCBI36
NG_031813.1:g.67080C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2576C= MANE Select	ENSP00000382717.3:p.Ala859=
ENST00000399820.7:c.2576C=	ENSP00000382717.3:p.Ala859=
ENST00000506869.5:c.*2157C=	ENSP00000424319.1:n.*2157C=
ENST00000512095.5:n.1574C=
NM_025132.3:c.2576C=	NP_079408.3:p.Ala859=
XM_011513724.1:c.2588C=	XP_011512026.1:p.Ala863=
XM_011513725.1:c.2522C=	XP_011512027.1:p.Ala841=
XM_011513726.1:c.2108C=	XP_011512028.1:p.Ala703=
XM_011513727.1:c.2108C=	XP_011512029.1:p.Ala703=
XM_011513728.1:c.2096C=	XP_011512030.1:p.Ala699=
XM_011513729.1:c.2588C=	XP_011512031.1:p.Ala863=
XR_925155.1:n.2652C=
NM_001317924.1:c.2096C=	NP_001304853.1:p.Ala699=
XM_011513725.2:c.2522C=	XP_011512027.1:p.Ala841=
XM_011513726.3:c.2108C=	XP_011512028.1:p.Ala703=
XM_017008501.1:c.2096C=	XP_016863990.1:p.Ala699=
XR_001741306.1:n.2652C=
XR_001741307.1:n.2640C=
XR_001741308.1:n.2652C=
XR_001741309.1:n.2640C=
XR_001741310.1:n.2640C=
XR_001741311.2:n.2489C=
NM_025132.4:c.2576C= MANE Select	NP_079408.3:p.Ala859=
NM_001317924.2:c.2096C=	NP_001304853.1:p.Ala699=