Canonical Allele Identifier: CA2670359584

Gene: WDR19

Linked Data

• gnomAD v4: 4-39244417-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244418_39244419insAT , CM000666.2:g.39244418_39244419insAT	GRCh38
NC_000004.11:g.39246038_39246039insAT , CM000666.1:g.39246038_39246039insAT	GRCh37
NC_000004.10:g.38922433_38922434insAT	NCBI36
NG_031813.1:g.67015_67016insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2562+30_2562+31insAT MANE Select	ENSP00000382717.3:n.2562+30_2562+31insAT
ENST00000399820.7:c.2562+30_2562+31insAT	ENSP00000382717.3:n.2562+30_2562+31insAT
ENST00000506869.5:c.*2143+30_*2143+31insAT	ENSP00000424319.1:n.*2143+30_*2143+31insAT
ENST00000512095.5:n.1560+30_1560+31insAT
NM_025132.3:c.2562+30_2562+31insAT	NP_079408.3:n.2562+30_2562+31insAT
XM_011513724.1:c.2574+30_2574+31insAT	XP_011512026.1:n.2574+30_2574+31insAT
XM_011513725.1:c.2508+30_2508+31insAT	XP_011512027.1:n.2508+30_2508+31insAT
XM_011513726.1:c.2094+30_2094+31insAT	XP_011512028.1:n.2094+30_2094+31insAT
XM_011513727.1:c.2094+30_2094+31insAT	XP_011512029.1:n.2094+30_2094+31insAT
XM_011513728.1:c.2082+30_2082+31insAT	XP_011512030.1:n.2082+30_2082+31insAT
XM_011513729.1:c.2574+30_2574+31insAT	XP_011512031.1:n.2574+30_2574+31insAT
XR_925155.1:n.2638+30_2638+31insAT
NM_001317924.1:c.2082+30_2082+31insAT	NP_001304853.1:n.2082+30_2082+31insAT
XM_011513725.2:c.2508+30_2508+31insAT	XP_011512027.1:n.2508+30_2508+31insAT
XM_011513726.3:c.2094+30_2094+31insAT	XP_011512028.1:n.2094+30_2094+31insAT
XM_017008501.1:c.2082+30_2082+31insAT	XP_016863990.1:n.2082+30_2082+31insAT
XR_001741306.1:n.2638+30_2638+31insAT
XR_001741307.1:n.2626+30_2626+31insAT
XR_001741308.1:n.2638+30_2638+31insAT
XR_001741309.1:n.2626+30_2626+31insAT
XR_001741310.1:n.2626+30_2626+31insAT
XR_001741311.2:n.2475+30_2475+31insAT
NM_025132.4:c.2562+30_2562+31insAT MANE Select	NP_079408.3:n.2562+30_2562+31insAT
NM_001317924.2:c.2082+30_2082+31insAT	NP_001304853.1:n.2082+30_2082+31insAT