Canonical Allele Identifier: CA2761112712

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205346_39205347insT , CM000666.2:g.39205346_39205347insT	GRCh38
NC_000004.11:g.39206966_39206967insT , CM000666.1:g.39206966_39206967insT	GRCh37
NC_000004.10:g.38883361_38883362insT	NCBI36
NG_031813.1:g.27943_27944insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.716+80_716+81insT MANE Select	ENSP00000382717.3:n.716+80_716+81insT
ENST00000399820.7:c.716+80_716+81insT	ENSP00000382717.3:n.716+80_716+81insT
ENST00000503697.5:c.*184+80_*184+81insT	ENSP00000423706.1:n.*184+80_*184+81insT
ENST00000505055.5:c.*297+80_*297+81insT	ENSP00000425949.1:n.*297+80_*297+81insT
ENST00000506503.1:c.716+80_716+81insT	ENSP00000423491.1:n.716+80_716+81insT
ENST00000506869.5:c.*297+80_*297+81insT	ENSP00000424319.1:n.*297+80_*297+81insT
ENST00000511729.5:n.40+22783_40+22784insT
ENST00000512448.1:n.310+80_310+81insT
NM_025132.3:c.716+80_716+81insT	NP_079408.3:n.716+80_716+81insT
XM_011513724.1:c.716+80_716+81insT	XP_011512026.1:n.716+80_716+81insT
XM_011513725.1:c.650+80_650+81insT	XP_011512027.1:n.650+80_650+81insT
XM_011513726.1:c.236+80_236+81insT	XP_011512028.1:n.236+80_236+81insT
XM_011513727.1:c.236+80_236+81insT	XP_011512029.1:n.236+80_236+81insT
XM_011513728.1:c.236+80_236+81insT	XP_011512030.1:n.236+80_236+81insT
XM_011513729.1:c.716+80_716+81insT	XP_011512031.1:n.716+80_716+81insT
XR_925155.1:n.780+80_780+81insT
NM_001317924.1:c.236+80_236+81insT	NP_001304853.1:n.236+80_236+81insT
XM_011513725.2:c.650+80_650+81insT	XP_011512027.1:n.650+80_650+81insT
XM_011513726.3:c.236+80_236+81insT	XP_011512028.1:n.236+80_236+81insT
XM_017008501.1:c.236+80_236+81insT	XP_016863990.1:n.236+80_236+81insT
XR_001741306.1:n.780+80_780+81insT
XR_001741307.1:n.780+80_780+81insT
XR_001741308.1:n.780+80_780+81insT
XR_001741309.1:n.780+80_780+81insT
XR_001741310.1:n.780+80_780+81insT
XR_001741311.2:n.629+80_629+81insT
XR_001741312.1:n.780+80_780+81insT
NM_025132.4:c.716+80_716+81insT MANE Select	NP_079408.3:n.716+80_716+81insT
NM_001317924.2:c.236+80_236+81insT	NP_001304853.1:n.236+80_236+81insT