Canonical Allele Identifier: CA2891682

Gene: WDR19

Linked Data

• dbSNP Id: rs768993752
• ExAC: 4:39207161 AT / A
• gnomAD v2: 4-39207161-AT-A
• gnomAD v4: 4-39205541-AT-A
• MyVariant Identifiers: chr4:g.39207162del (hg19) ; chr4:g.39205542del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205543del , CM000666.2:g.39205543del	GRCh38
NC_000004.11:g.39207163del , CM000666.1:g.39207163del	GRCh37
NC_000004.10:g.38883558del	NCBI36
NG_031813.1:g.28140del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.717-20del MANE Select	ENSP00000382717.3:n.717-20del
ENST00000399820.7:c.717-20del	ENSP00000382717.3:n.717-20del
ENST00000503697.5:c.*185-20del	ENSP00000423706.1:n.*185-20del
ENST00000505055.5:c.*298-20del	ENSP00000425949.1:n.*298-20del
ENST00000506503.1:c.717-20del	ENSP00000423491.1:n.717-20del
ENST00000506869.5:c.*298-20del	ENSP00000424319.1:n.*298-20del
ENST00000511729.5:n.40+22980del
ENST00000512448.1:n.311-20del
NM_025132.3:c.717-20del	NP_079408.3:n.717-20del
XM_011513724.1:c.717-20del	XP_011512026.1:n.717-20del
XM_011513725.1:c.651-20del	XP_011512027.1:n.651-20del
XM_011513726.1:c.237-20del	XP_011512028.1:n.237-20del
XM_011513727.1:c.237-20del	XP_011512029.1:n.237-20del
XM_011513728.1:c.237-20del	XP_011512030.1:n.237-20del
XM_011513729.1:c.717-20del	XP_011512031.1:n.717-20del
XR_925155.1:n.781-20del
NM_001317924.1:c.237-20del	NP_001304853.1:n.237-20del
XM_011513725.2:c.651-20del	XP_011512027.1:n.651-20del
XM_011513726.3:c.237-20del	XP_011512028.1:n.237-20del
XM_017008501.1:c.237-20del	XP_016863990.1:n.237-20del
XR_001741306.1:n.781-20del
XR_001741307.1:n.781-20del
XR_001741308.1:n.781-20del
XR_001741309.1:n.781-20del
XR_001741310.1:n.781-20del
XR_001741311.2:n.630-20del
XR_001741312.1:n.781-20del
NM_025132.4:c.717-20del MANE Select	NP_079408.3:n.717-20del
NM_001317924.2:c.237-20del	NP_001304853.1:n.237-20del