Canonical Allele Identifier: CA2670359591

Gene: WDR19

Linked Data

• gnomAD v4: 4-39244428-T-TAC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244430_39244431dup , CM000666.2:g.39244430_39244431dup	GRCh38
NC_000004.11:g.39246050_39246051dup , CM000666.1:g.39246050_39246051dup	GRCh37
NC_000004.10:g.38922445_38922446dup	NCBI36
NG_031813.1:g.67027_67028dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2563-40_2563-39dup MANE Select	ENSP00000382717.3:n.2563-40_2563-39dup
ENST00000399820.7:c.2563-40_2563-39dup	ENSP00000382717.3:n.2563-40_2563-39dup
ENST00000506869.5:c.*2144-40_*2144-39dup	ENSP00000424319.1:n.*2144-40_*2144-39dup
ENST00000512095.5:n.1561-40_1561-39dup
NM_025132.3:c.2563-40_2563-39dup	NP_079408.3:n.2563-40_2563-39dup
XM_011513724.1:c.2575-40_2575-39dup	XP_011512026.1:n.2575-40_2575-39dup
XM_011513725.1:c.2509-40_2509-39dup	XP_011512027.1:n.2509-40_2509-39dup
XM_011513726.1:c.2095-40_2095-39dup	XP_011512028.1:n.2095-40_2095-39dup
XM_011513727.1:c.2095-40_2095-39dup	XP_011512029.1:n.2095-40_2095-39dup
XM_011513728.1:c.2083-40_2083-39dup	XP_011512030.1:n.2083-40_2083-39dup
XM_011513729.1:c.2575-40_2575-39dup	XP_011512031.1:n.2575-40_2575-39dup
XR_925155.1:n.2639-40_2639-39dup
NM_001317924.1:c.2083-40_2083-39dup	NP_001304853.1:n.2083-40_2083-39dup
XM_011513725.2:c.2509-40_2509-39dup	XP_011512027.1:n.2509-40_2509-39dup
XM_011513726.3:c.2095-40_2095-39dup	XP_011512028.1:n.2095-40_2095-39dup
XM_017008501.1:c.2083-40_2083-39dup	XP_016863990.1:n.2083-40_2083-39dup
XR_001741306.1:n.2639-40_2639-39dup
XR_001741307.1:n.2627-40_2627-39dup
XR_001741308.1:n.2639-40_2639-39dup
XR_001741309.1:n.2627-40_2627-39dup
XR_001741310.1:n.2627-40_2627-39dup
XR_001741311.2:n.2476-40_2476-39dup
NM_025132.4:c.2563-40_2563-39dup MANE Select	NP_079408.3:n.2563-40_2563-39dup
NM_001317924.2:c.2083-40_2083-39dup	NP_001304853.1:n.2083-40_2083-39dup