Canonical Allele Identifier: CA1451994907

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205735_39205736delinsTG , CM000666.2:g.39205735_39205736delinsTG	GRCh38
NC_000004.11:g.39207355_39207356delinsTG , CM000666.1:g.39207355_39207356delinsTG	GRCh37
NC_000004.10:g.38883750_38883751delinsTG	NCBI36
NG_031813.1:g.28332_28333delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.889_890delinsTG MANE Select	ENSP00000382717.3:p.Cys297=
ENST00000399820.7:c.889_890delinsTG	ENSP00000382717.3:p.Cys297=
ENST00000503697.5:c.*357_*358delinsTG	ENSP00000423706.1:n.*357_*358delinsTG
ENST00000506503.1:c.889_890delinsTG	ENSP00000423491.1:p.Cys297=
ENST00000506869.5:c.*470_*471delinsTG	ENSP00000424319.1:n.*470_*471delinsTG
ENST00000511729.5:n.41-22823_41-22822delinsTG
ENST00000512448.1:n.483_484delinsTG
NM_025132.3:c.889_890delinsTG	NP_079408.3:p.Cys297=
XM_011513724.1:c.889_890delinsTG	XP_011512026.1:p.Cys297=
XM_011513725.1:c.823_824delinsTG	XP_011512027.1:p.Cys275=
XM_011513726.1:c.409_410delinsTG	XP_011512028.1:p.Cys137=
XM_011513727.1:c.409_410delinsTG	XP_011512029.1:p.Cys137=
XM_011513728.1:c.409_410delinsTG	XP_011512030.1:p.Cys137=
XM_011513729.1:c.889_890delinsTG	XP_011512031.1:p.Cys297=
XR_925155.1:n.953_954delinsTG
NM_001317924.1:c.409_410delinsTG	NP_001304853.1:p.Cys137=
XM_011513725.2:c.823_824delinsTG	XP_011512027.1:p.Cys275=
XM_011513726.3:c.409_410delinsTG	XP_011512028.1:p.Cys137=
XM_017008501.1:c.409_410delinsTG	XP_016863990.1:p.Cys137=
XR_001741306.1:n.953_954delinsTG
XR_001741307.1:n.953_954delinsTG
XR_001741308.1:n.953_954delinsTG
XR_001741309.1:n.953_954delinsTG
XR_001741310.1:n.953_954delinsTG
XR_001741311.2:n.802_803delinsTG
XR_001741312.1:n.953_954delinsTG
NM_025132.4:c.889_890delinsTG MANE Select	NP_079408.3:p.Cys297=
NM_001317924.2:c.409_410delinsTG	NP_001304853.1:p.Cys137=