Canonical Allele Identifier: CA1451994750

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205652T= , CM000666.2:g.39205652T=	GRCh38
NC_000004.11:g.39207272T= , CM000666.1:g.39207272T=	GRCh37
NC_000004.10:g.38883667T=	NCBI36
NG_031813.1:g.28249T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.806T= MANE Select	ENSP00000382717.3:p.Phe269=
ENST00000399820.7:c.806T=	ENSP00000382717.3:p.Phe269=
ENST00000503697.5:c.*274T=	ENSP00000423706.1:n.*274T=
ENST00000506503.1:c.806T=	ENSP00000423491.1:p.Phe269=
ENST00000506869.5:c.*387T=	ENSP00000424319.1:n.*387T=
ENST00000511729.5:n.41-22906T=
ENST00000512448.1:n.400T=
NM_025132.3:c.806T=	NP_079408.3:p.Phe269=
XM_011513724.1:c.806T=	XP_011512026.1:p.Phe269=
XM_011513725.1:c.740T=	XP_011512027.1:p.Phe247=
XM_011513726.1:c.326T=	XP_011512028.1:p.Phe109=
XM_011513727.1:c.326T=	XP_011512029.1:p.Phe109=
XM_011513728.1:c.326T=	XP_011512030.1:p.Phe109=
XM_011513729.1:c.806T=	XP_011512031.1:p.Phe269=
XR_925155.1:n.870T=
NM_001317924.1:c.326T=	NP_001304853.1:p.Phe109=
XM_011513725.2:c.740T=	XP_011512027.1:p.Phe247=
XM_011513726.3:c.326T=	XP_011512028.1:p.Phe109=
XM_017008501.1:c.326T=	XP_016863990.1:p.Phe109=
XR_001741306.1:n.870T=
XR_001741307.1:n.870T=
XR_001741308.1:n.870T=
XR_001741309.1:n.870T=
XR_001741310.1:n.870T=
XR_001741311.2:n.719T=
XR_001741312.1:n.870T=
NM_025132.4:c.806T= MANE Select	NP_079408.3:p.Phe269=
NM_001317924.2:c.326T=	NP_001304853.1:p.Phe109=