Canonical Allele Identifier: CA2761116525

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39276931_39276932insACT , CM000666.2:g.39276931_39276932insACT	GRCh38
NC_000004.11:g.39278551_39278552insACT , CM000666.1:g.39278551_39278552insACT	GRCh37
NC_000004.10:g.38954946_38954947insACT	NCBI36
NG_031813.1:g.99528_99529insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3717-89_3717-88insACT MANE Select	ENSP00000382717.3:n.3717-89_3717-88insACT
ENST00000399820.7:c.3717-89_3717-88insACT	ENSP00000382717.3:n.3717-89_3717-88insACT
ENST00000506869.5:c.*3298-89_*3298-88insACT	ENSP00000424319.1:n.*3298-89_*3298-88insACT
ENST00000512534.5:n.2028-89_2028-88insACT
NM_025132.3:c.3717-89_3717-88insACT	NP_079408.3:n.3717-89_3717-88insACT
XM_011513724.1:c.3729-89_3729-88insACT	XP_011512026.1:n.3729-89_3729-88insACT
XM_011513725.1:c.3663-89_3663-88insACT	XP_011512027.1:n.3663-89_3663-88insACT
XM_011513726.1:c.3249-89_3249-88insACT	XP_011512028.1:n.3249-89_3249-88insACT
XM_011513727.1:c.3249-89_3249-88insACT	XP_011512029.1:n.3249-89_3249-88insACT
XM_011513728.1:c.3237-89_3237-88insACT	XP_011512030.1:n.3237-89_3237-88insACT
XR_925155.1:n.5427-89_5427-88insACT
NM_001317924.1:c.3237-89_3237-88insACT	NP_001304853.1:n.3237-89_3237-88insACT
XM_011513725.2:c.3663-89_3663-88insACT	XP_011512027.1:n.3663-89_3663-88insACT
XM_011513726.3:c.3249-89_3249-88insACT	XP_011512028.1:n.3249-89_3249-88insACT
XM_017008501.1:c.3237-89_3237-88insACT	XP_016863990.1:n.3237-89_3237-88insACT
XR_001741306.1:n.3993+52_3993+53insACT
XR_001741307.1:n.3981+52_3981+53insACT
XR_001741308.1:n.5627+52_5627+53insACT
XR_001741309.1:n.5415-89_5415-88insACT
XR_001741310.1:n.5615+52_5615+53insACT
XR_001741311.2:n.5264-89_5264-88insACT
NM_025132.4:c.3717-89_3717-88insACT MANE Select	NP_079408.3:n.3717-89_3717-88insACT
NM_001317924.2:c.3237-89_3237-88insACT	NP_001304853.1:n.3237-89_3237-88insACT