Canonical Allele Identifier: CA2670363049

Gene: WDR19

Linked Data

• gnomAD v4: 4-39277018-A-ATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277018_39277019insTCC , CM000666.2:g.39277018_39277019insTCC	GRCh38
NC_000004.11:g.39278638_39278639insTCC , CM000666.1:g.39278638_39278639insTCC	GRCh37
NC_000004.10:g.38955033_38955034insTCC	NCBI36
NG_031813.1:g.99615_99616insTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3717-2_3717-1insTCC MANE Select	ENSP00000382717.3:n.3717-2_3717-1insTCC
ENST00000399820.7:c.3717-2_3717-1insTCC	ENSP00000382717.3:n.3717-2_3717-1insTCC
ENST00000503733.1:n.55_56insTCC
ENST00000506869.5:c.*3298-2_*3298-1insTCC	ENSP00000424319.1:n.*3298-2_*3298-1insTCC...
ENST00000512534.5:n.2028-2_2028-1insTCC
ENST00000512588.5:n.57_58insTCC
NM_025132.3:c.3717-2_3717-1insTCC	NP_079408.3:n.3717-2_3717-1insTCC
XM_011513724.1:c.3729-2_3729-1insTCC	XP_011512026.1:n.3729-2_3729-1insTCC
XM_011513725.1:c.3663-2_3663-1insTCC	XP_011512027.1:n.3663-2_3663-1insTCC
XM_011513726.1:c.3249-2_3249-1insTCC	XP_011512028.1:n.3249-2_3249-1insTCC
XM_011513727.1:c.3249-2_3249-1insTCC	XP_011512029.1:n.3249-2_3249-1insTCC
XM_011513728.1:c.3237-2_3237-1insTCC	XP_011512030.1:n.3237-2_3237-1insTCC
XR_925155.1:n.5427-2_5427-1insTCC
NM_001317924.1:c.3237-2_3237-1insTCC	NP_001304853.1:n.3237-2_3237-1insTCC
XM_011513725.2:c.3663-2_3663-1insTCC	XP_011512027.1:n.3663-2_3663-1insTCC
XM_011513726.3:c.3249-2_3249-1insTCC	XP_011512028.1:n.3249-2_3249-1insTCC
XM_017008501.1:c.3237-2_3237-1insTCC	XP_016863990.1:n.3237-2_3237-1insTCC
XR_001741306.1:n.3994-2_3994-1insTCC
XR_001741307.1:n.3982-2_3982-1insTCC
XR_001741308.1:n.5628-2_5628-1insTCC
XR_001741309.1:n.5415-2_5415-1insTCC
XR_001741310.1:n.5616-2_5616-1insTCC
XR_001741311.2:n.5264-2_5264-1insTCC
NM_025132.4:c.3717-2_3717-1insTCC MANE Select	NP_079408.3:n.3717-2_3717-1insTCC
NM_001317924.2:c.3237-2_3237-1insTCC	NP_001304853.1:n.3237-2_3237-1insTCC