Canonical Allele Identifier: CA2670359590

Gene: WDR19

Linked Data

• gnomAD v4: 4-39244427-ATACAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244428_39244432del , CM000666.2:g.39244428_39244432del	GRCh38
NC_000004.11:g.39246048_39246052del , CM000666.1:g.39246048_39246052del	GRCh37
NC_000004.10:g.38922443_38922447del	NCBI36
NG_031813.1:g.67025_67029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2562+40_2563-38del MANE Select	ENSP00000382717.3:n.2562+40_2563-38del
ENST00000399820.7:c.2562+40_2563-38del	ENSP00000382717.3:n.2562+40_2563-38del
ENST00000506869.5:c.*2143+40_*2144-38del	ENSP00000424319.1:n.*2143+40_*2144-38del
ENST00000512095.5:n.1560+40_1561-38del
NM_025132.3:c.2562+40_2563-38del	NP_079408.3:n.2562+40_2563-38del
XM_011513724.1:c.2574+40_2575-38del	XP_011512026.1:n.2574+40_2575-38del
XM_011513725.1:c.2508+40_2509-38del	XP_011512027.1:n.2508+40_2509-38del
XM_011513726.1:c.2094+40_2095-38del	XP_011512028.1:n.2094+40_2095-38del
XM_011513727.1:c.2094+40_2095-38del	XP_011512029.1:n.2094+40_2095-38del
XM_011513728.1:c.2082+40_2083-38del	XP_011512030.1:n.2082+40_2083-38del
XM_011513729.1:c.2574+40_2575-38del	XP_011512031.1:n.2574+40_2575-38del
XR_925155.1:n.2638+40_2639-38del
NM_001317924.1:c.2082+40_2083-38del	NP_001304853.1:n.2082+40_2083-38del
XM_011513725.2:c.2508+40_2509-38del	XP_011512027.1:n.2508+40_2509-38del
XM_011513726.3:c.2094+40_2095-38del	XP_011512028.1:n.2094+40_2095-38del
XM_017008501.1:c.2082+40_2083-38del	XP_016863990.1:n.2082+40_2083-38del
XR_001741306.1:n.2638+40_2639-38del
XR_001741307.1:n.2626+40_2627-38del
XR_001741308.1:n.2638+40_2639-38del
XR_001741309.1:n.2626+40_2627-38del
XR_001741310.1:n.2626+40_2627-38del
XR_001741311.2:n.2475+40_2476-38del
NM_025132.4:c.2562+40_2563-38del MANE Select	NP_079408.3:n.2562+40_2563-38del
NM_001317924.2:c.2082+40_2083-38del	NP_001304853.1:n.2082+40_2083-38del