Canonical Allele Identifier: CA1452058469

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277011_39277012delinsTC , CM000666.2:g.39277011_39277012delinsTC	GRCh38
NC_000004.11:g.39278631_39278632delinsTC , CM000666.1:g.39278631_39278632delinsTC	GRCh37
NC_000004.10:g.38955026_38955027delinsTC	NCBI36
NG_031813.1:g.99608_99609delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3717-9_3717-8delinsTC MANE Select	ENSP00000382717.3:n.3717-9_3717-8delinsTC...
ENST00000399820.7:c.3717-9_3717-8delinsTC	ENSP00000382717.3:n.3717-9_3717-8delinsTC...
ENST00000503733.1:n.48_49delinsTC
ENST00000506869.5:c.*3298-9_*3298-8delinsTC	ENSP00000424319.1:n.*3298-9_*3298-8delins...
ENST00000512534.5:n.2028-9_2028-8delinsTC
ENST00000512588.5:n.50_51delinsTC
NM_025132.3:c.3717-9_3717-8delinsTC	NP_079408.3:n.3717-9_3717-8delinsTC
XM_011513724.1:c.3729-9_3729-8delinsTC	XP_011512026.1:n.3729-9_3729-8delinsTC
XM_011513725.1:c.3663-9_3663-8delinsTC	XP_011512027.1:n.3663-9_3663-8delinsTC
XM_011513726.1:c.3249-9_3249-8delinsTC	XP_011512028.1:n.3249-9_3249-8delinsTC
XM_011513727.1:c.3249-9_3249-8delinsTC	XP_011512029.1:n.3249-9_3249-8delinsTC
XM_011513728.1:c.3237-9_3237-8delinsTC	XP_011512030.1:n.3237-9_3237-8delinsTC
XR_925155.1:n.5427-9_5427-8delinsTC
NM_001317924.1:c.3237-9_3237-8delinsTC	NP_001304853.1:n.3237-9_3237-8delinsTC
XM_011513725.2:c.3663-9_3663-8delinsTC	XP_011512027.1:n.3663-9_3663-8delinsTC
XM_011513726.3:c.3249-9_3249-8delinsTC	XP_011512028.1:n.3249-9_3249-8delinsTC
XM_017008501.1:c.3237-9_3237-8delinsTC	XP_016863990.1:n.3237-9_3237-8delinsTC
XR_001741306.1:n.3994-9_3994-8delinsTC
XR_001741307.1:n.3982-9_3982-8delinsTC
XR_001741308.1:n.5628-9_5628-8delinsTC
XR_001741309.1:n.5415-9_5415-8delinsTC
XR_001741310.1:n.5616-9_5616-8delinsTC
XR_001741311.2:n.5264-9_5264-8delinsTC
NM_025132.4:c.3717-9_3717-8delinsTC MANE Select	NP_079408.3:n.3717-9_3717-8delinsTC
NM_001317924.2:c.3237-9_3237-8delinsTC	NP_001304853.1:n.3237-9_3237-8delinsTC