Canonical Allele Identifier: CA2892466

Gene: WDR19

Linked Data

• dbSNP Id: rs758407111
• ExAC: 4:39278631 TC / T
• gnomAD v2: 4-39278631-TC-T
• gnomAD v4: 4-39277011-TC-T
• MyVariant Identifiers: chr4:g.39278632del (hg19) ; chr4:g.39277012del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277013del , CM000666.2:g.39277013del	GRCh38
NC_000004.11:g.39278633del , CM000666.1:g.39278633del	GRCh37
NC_000004.10:g.38955028del	NCBI36
NG_031813.1:g.99610del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3717-7del MANE Select	ENSP00000382717.3:n.3717-7del
ENST00000399820.7:c.3717-7del	ENSP00000382717.3:n.3717-7del
ENST00000503733.1:n.50del
ENST00000506869.5:c.*3298-7del	ENSP00000424319.1:n.*3298-7del
ENST00000512534.5:n.2028-7del
ENST00000512588.5:n.52del
NM_025132.3:c.3717-7del	NP_079408.3:n.3717-7del
XM_011513724.1:c.3729-7del	XP_011512026.1:n.3729-7del
XM_011513725.1:c.3663-7del	XP_011512027.1:n.3663-7del
XM_011513726.1:c.3249-7del	XP_011512028.1:n.3249-7del
XM_011513727.1:c.3249-7del	XP_011512029.1:n.3249-7del
XM_011513728.1:c.3237-7del	XP_011512030.1:n.3237-7del
XR_925155.1:n.5427-7del
NM_001317924.1:c.3237-7del	NP_001304853.1:n.3237-7del
XM_011513725.2:c.3663-7del	XP_011512027.1:n.3663-7del
XM_011513726.3:c.3249-7del	XP_011512028.1:n.3249-7del
XM_017008501.1:c.3237-7del	XP_016863990.1:n.3237-7del
XR_001741306.1:n.3994-7del
XR_001741307.1:n.3982-7del
XR_001741308.1:n.5628-7del
XR_001741309.1:n.5415-7del
XR_001741310.1:n.5616-7del
XR_001741311.2:n.5264-7del
NM_025132.4:c.3717-7del MANE Select	NP_079408.3:n.3717-7del
NM_001317924.2:c.3237-7del	NP_001304853.1:n.3237-7del