Canonical Allele Identifier: CA1451994249

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205184T= , CM000666.2:g.39205184T=	GRCh38
NC_000004.11:g.39206804T= , CM000666.1:g.39206804T=	GRCh37
NC_000004.10:g.38883199T=	NCBI36
NG_031813.1:g.27781T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.634T= MANE Select	ENSP00000382717.3:p.Phe212=
ENST00000399820.7:c.634T=	ENSP00000382717.3:p.Phe212=
ENST00000503697.5:c.*102T=	ENSP00000423706.1:n.*102T=
ENST00000505055.5:c.*215T=	ENSP00000425949.1:n.*215T=
ENST00000506503.1:c.634T=	ENSP00000423491.1:p.Phe212=
ENST00000506869.5:c.*215T=	ENSP00000424319.1:n.*215T=
ENST00000511729.5:n.40+22621T=
ENST00000512448.1:n.228T=
NM_025132.3:c.634T=	NP_079408.3:p.Phe212=
XM_011513724.1:c.634T=	XP_011512026.1:p.Phe212=
XM_011513725.1:c.568T=	XP_011512027.1:p.Phe190=
XM_011513726.1:c.154T=	XP_011512028.1:p.Phe52=
XM_011513727.1:c.154T=	XP_011512029.1:p.Phe52=
XM_011513728.1:c.154T=	XP_011512030.1:p.Phe52=
XM_011513729.1:c.634T=	XP_011512031.1:p.Phe212=
XR_925155.1:n.698T=
NM_001317924.1:c.154T=	NP_001304853.1:p.Phe52=
XM_011513725.2:c.568T=	XP_011512027.1:p.Phe190=
XM_011513726.3:c.154T=	XP_011512028.1:p.Phe52=
XM_017008501.1:c.154T=	XP_016863990.1:p.Phe52=
XR_001741306.1:n.698T=
XR_001741307.1:n.698T=
XR_001741308.1:n.698T=
XR_001741309.1:n.698T=
XR_001741310.1:n.698T=
XR_001741311.2:n.547T=
XR_001741312.1:n.698T=
NM_025132.4:c.634T= MANE Select	NP_079408.3:p.Phe212=
NM_001317924.2:c.154T=	NP_001304853.1:p.Phe52=