Canonical Allele Identifier: CA1452055148

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273012G= , CM000666.2:g.39273012G=	GRCh38
NC_000004.11:g.39274632G= , CM000666.1:g.39274632G=	GRCh37
NC_000004.10:g.38951027G=	NCBI36
NG_031813.1:g.95609G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3516G= MANE Select	ENSP00000382717.3:p.Gly1172=
ENST00000399820.7:c.3516G=	ENSP00000382717.3:p.Gly1172=
ENST00000506869.5:c.*3097G=	ENSP00000424319.1:n.*3097G=
ENST00000512095.5:n.2514G=
ENST00000512534.5:n.81G=
NM_025132.3:c.3516G=	NP_079408.3:p.Gly1172=
XM_011513724.1:c.3528G=	XP_011512026.1:p.Gly1176=
XM_011513725.1:c.3462G=	XP_011512027.1:p.Gly1154=
XM_011513726.1:c.3048G=	XP_011512028.1:p.Gly1016=
XM_011513727.1:c.3048G=	XP_011512029.1:p.Gly1016=
XM_011513728.1:c.3036G=	XP_011512030.1:p.Gly1012=
XR_925155.1:n.3592G=
NM_001317924.1:c.3036G=	NP_001304853.1:p.Gly1012=
XM_011513725.2:c.3462G=	XP_011512027.1:p.Gly1154=
XM_011513726.3:c.3048G=	XP_011512028.1:p.Gly1016=
XM_017008501.1:c.3036G=	XP_016863990.1:p.Gly1012=
XR_001741306.1:n.3592G=
XR_001741307.1:n.3580G=
XR_001741308.1:n.3592G=
XR_001741309.1:n.3580G=
XR_001741310.1:n.3580G=
XR_001741311.2:n.3429G=
NM_025132.4:c.3516G= MANE Select	NP_079408.3:p.Gly1172=
NM_001317924.2:c.3036G=	NP_001304853.1:p.Gly1012=