Canonical Allele Identifier: CA10620963

Gene: WDR19

Linked Data

• ClinVar Variation Id: 348721
• ClinVar RCV Id: RCV000261825 ; RCV000375119
• dbSNP Id: rs558898928
• gnomAD v2: 4-39184117-C-CT
• gnomAD v3: 4-39182497-C-CT
• gnomAD v4: 4-39182497-C-CT
• MyVariant Identifiers: chr4:g.39184119dupT (hg19) ; chr4:g.39184117_39184118insT (hg19) ; chr4:g.39182499dupT (hg38) ; chr4:g.39182497_39182498insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39182499dup , CM000666.2:g.39182499dup	GRCh38
NC_000004.11:g.39184119dup , CM000666.1:g.39184119dup	GRCh37
NC_000004.10:g.38860514dup	NCBI36
NG_031813.1:g.5096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.7:c.-59dup	ENSP00000382717.3:n.-59dup
NM_025132.3:c.-59dup	NP_079408.3:n.-59dup
XM_011513724.1:c.-59dup	XP_011512026.1:n.-59dup
XM_011513725.1:c.-59dup	XP_011512027.1:n.-59dup
XM_011513729.1:c.-59dup	XP_011512031.1:n.-59dup
XR_925155.1:n.6dup
NM_001317924.1:c.-423dup	NP_001304853.1:n.-423dup
XM_011513725.2:c.-59dup	XP_011512027.1:n.-59dup
XR_001741306.1:n.6dup
XR_001741307.1:n.6dup
XR_001741308.1:n.6dup
XR_001741309.1:n.6dup
XR_001741310.1:n.6dup
XR_001741312.1:n.6dup