Canonical Allele Identifier: CA1452055168

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39273022C= , CM000666.2:g.39273022C=	GRCh38
NC_000004.11:g.39274642C= , CM000666.1:g.39274642C=	GRCh37
NC_000004.10:g.38951037C=	NCBI36
NG_031813.1:g.95619C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3526C= MANE Select	ENSP00000382717.3:p.Leu1176=
ENST00000399820.7:c.3526C=	ENSP00000382717.3:p.Leu1176=
ENST00000506869.5:c.*3107C=	ENSP00000424319.1:n.*3107C=
ENST00000512095.5:n.2524C=
ENST00000512534.5:n.91C=
NM_025132.3:c.3526C=	NP_079408.3:p.Leu1176=
XM_011513724.1:c.3538C=	XP_011512026.1:p.Leu1180=
XM_011513725.1:c.3472C=	XP_011512027.1:p.Leu1158=
XM_011513726.1:c.3058C=	XP_011512028.1:p.Leu1020=
XM_011513727.1:c.3058C=	XP_011512029.1:p.Leu1020=
XM_011513728.1:c.3046C=	XP_011512030.1:p.Leu1016=
XR_925155.1:n.3602C=
NM_001317924.1:c.3046C=	NP_001304853.1:p.Leu1016=
XM_011513725.2:c.3472C=	XP_011512027.1:p.Leu1158=
XM_011513726.3:c.3058C=	XP_011512028.1:p.Leu1020=
XM_017008501.1:c.3046C=	XP_016863990.1:p.Leu1016=
XR_001741306.1:n.3602C=
XR_001741307.1:n.3590C=
XR_001741308.1:n.3602C=
XR_001741309.1:n.3590C=
XR_001741310.1:n.3590C=
XR_001741311.2:n.3439C=
NM_025132.4:c.3526C= MANE Select	NP_079408.3:p.Leu1176=
NM_001317924.2:c.3046C=	NP_001304853.1:p.Leu1016=