Canonical Allele Identifier: CA1451994736

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205647G= , CM000666.2:g.39205647G=	GRCh38
NC_000004.11:g.39207267G= , CM000666.1:g.39207267G=	GRCh37
NC_000004.10:g.38883662G=	NCBI36
NG_031813.1:g.28244G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.801G= MANE Select	ENSP00000382717.3:p.Glu267=
ENST00000399820.7:c.801G=	ENSP00000382717.3:p.Glu267=
ENST00000503697.5:c.*269G=	ENSP00000423706.1:n.*269G=
ENST00000506503.1:c.801G=	ENSP00000423491.1:p.Glu267=
ENST00000506869.5:c.*382G=	ENSP00000424319.1:n.*382G=
ENST00000511729.5:n.41-22911G=
ENST00000512448.1:n.395G=
NM_025132.3:c.801G=	NP_079408.3:p.Glu267=
XM_011513724.1:c.801G=	XP_011512026.1:p.Glu267=
XM_011513725.1:c.735G=	XP_011512027.1:p.Glu245=
XM_011513726.1:c.321G=	XP_011512028.1:p.Glu107=
XM_011513727.1:c.321G=	XP_011512029.1:p.Glu107=
XM_011513728.1:c.321G=	XP_011512030.1:p.Glu107=
XM_011513729.1:c.801G=	XP_011512031.1:p.Glu267=
XR_925155.1:n.865G=
NM_001317924.1:c.321G=	NP_001304853.1:p.Glu107=
XM_011513725.2:c.735G=	XP_011512027.1:p.Glu245=
XM_011513726.3:c.321G=	XP_011512028.1:p.Glu107=
XM_017008501.1:c.321G=	XP_016863990.1:p.Glu107=
XR_001741306.1:n.865G=
XR_001741307.1:n.865G=
XR_001741308.1:n.865G=
XR_001741309.1:n.865G=
XR_001741310.1:n.865G=
XR_001741311.2:n.714G=
XR_001741312.1:n.865G=
NM_025132.4:c.801G= MANE Select	NP_079408.3:p.Glu267=
NM_001317924.2:c.321G=	NP_001304853.1:p.Glu107=