Canonical Allele Identifier: CA2891669

Gene: WDR19

Linked Data

• ClinVar Variation Id: 1158784
• ClinVar RCV Id: RCV001502315 ; RCV004540460
• dbSNP Id: rs747438345
• ExAC: 4:39206768 TGG / T
• gnomAD v2: 4-39206768-TGG-T
• gnomAD v3: 4-39205148-TGG-T
• gnomAD v4: 4-39205148-TGG-T
• MyVariant Identifiers: chr4:g.39206769_39206770del (hg19) ; chr4:g.39205149_39205150del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205149_39205150del , CM000666.2:g.39205149_39205150del	GRCh38
NC_000004.11:g.39206769_39206770del , CM000666.1:g.39206769_39206770del	GRCh37
NC_000004.10:g.38883164_38883165del	NCBI36
NG_031813.1:g.27746_27747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.604-5_604-4del MANE Select	ENSP00000382717.3:n.604-5_604-4del
ENST00000399820.7:c.604-5_604-4del	ENSP00000382717.3:n.604-5_604-4del
ENST00000503697.5:c.*72-5_*72-4del	ENSP00000423706.1:n.*72-5_*72-4del
ENST00000505055.5:c.*185-5_*185-4del	ENSP00000425949.1:n.*185-5_*185-4del
ENST00000506503.1:c.604-5_604-4del	ENSP00000423491.1:n.604-5_604-4del
ENST00000506869.5:c.*185-5_*185-4del	ENSP00000424319.1:n.*185-5_*185-4del
ENST00000511729.5:n.40+22586_40+22587del
ENST00000512448.1:n.198-5_198-4del
NM_025132.3:c.604-5_604-4del	NP_079408.3:n.604-5_604-4del
XM_011513724.1:c.604-5_604-4del	XP_011512026.1:n.604-5_604-4del
XM_011513725.1:c.538-5_538-4del	XP_011512027.1:n.538-5_538-4del
XM_011513726.1:c.124-5_124-4del	XP_011512028.1:n.124-5_124-4del
XM_011513727.1:c.124-5_124-4del	XP_011512029.1:n.124-5_124-4del
XM_011513728.1:c.124-5_124-4del	XP_011512030.1:n.124-5_124-4del
XM_011513729.1:c.604-5_604-4del	XP_011512031.1:n.604-5_604-4del
XR_925155.1:n.668-5_668-4del
NM_001317924.1:c.124-5_124-4del	NP_001304853.1:n.124-5_124-4del
XM_011513725.2:c.538-5_538-4del	XP_011512027.1:n.538-5_538-4del
XM_011513726.3:c.124-5_124-4del	XP_011512028.1:n.124-5_124-4del
XM_017008501.1:c.124-5_124-4del	XP_016863990.1:n.124-5_124-4del
XR_001741306.1:n.668-5_668-4del
XR_001741307.1:n.668-5_668-4del
XR_001741308.1:n.668-5_668-4del
XR_001741309.1:n.668-5_668-4del
XR_001741310.1:n.668-5_668-4del
XR_001741311.2:n.517-5_517-4del
XR_001741312.1:n.668-5_668-4del
NM_025132.4:c.604-5_604-4del MANE Select	NP_079408.3:n.604-5_604-4del
NM_001317924.2:c.124-5_124-4del	NP_001304853.1:n.124-5_124-4del