Canonical Allele Identifier: CA2761112828

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205727del , CM000666.2:g.39205727del	GRCh38
NC_000004.11:g.39207347del , CM000666.1:g.39207347del	GRCh37
NC_000004.10:g.38883742del	NCBI36
NG_031813.1:g.28324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.881del MANE Select	ENSP00000382717.3:p.Gly294GlufsTer13
ENST00000399820.7:c.881del	ENSP00000382717.3:p.Gly294GlufsTer13
ENST00000503697.5:c.*349del	ENSP00000423706.1:n.*349del
ENST00000506503.1:c.881del	ENSP00000423491.1:p.Gly294GlufsTer13
ENST00000506869.5:c.*462del	ENSP00000424319.1:n.*462del
ENST00000511729.5:n.41-22831del
ENST00000512448.1:n.475del
NM_025132.3:c.881del	NP_079408.3:p.Gly294GlufsTer13
XM_011513724.1:c.881del	XP_011512026.1:p.Gly294GlufsTer13
XM_011513725.1:c.815del	XP_011512027.1:p.Gly272GlufsTer13
XM_011513726.1:c.401del	XP_011512028.1:p.Gly134GlufsTer13
XM_011513727.1:c.401del	XP_011512029.1:p.Gly134GlufsTer13
XM_011513728.1:c.401del	XP_011512030.1:p.Gly134GlufsTer13
XM_011513729.1:c.881del	XP_011512031.1:p.Gly294GlufsTer13
XR_925155.1:n.945del
NM_001317924.1:c.401del	NP_001304853.1:p.Gly134GlufsTer13
XM_011513725.2:c.815del	XP_011512027.1:p.Gly272GlufsTer13
XM_011513726.3:c.401del	XP_011512028.1:p.Gly134GlufsTer13
XM_017008501.1:c.401del	XP_016863990.1:p.Gly134GlufsTer13
XR_001741306.1:n.945del
XR_001741307.1:n.945del
XR_001741308.1:n.945del
XR_001741309.1:n.945del
XR_001741310.1:n.945del
XR_001741311.2:n.794del
XR_001741312.1:n.945del
NM_025132.4:c.881del MANE Select	NP_079408.3:p.Gly294GlufsTer13
NM_001317924.2:c.401del	NP_001304853.1:p.Gly134GlufsTer13