Canonical Allele Identifier: CA2670356464

Gene: WDR19

Linked Data

• gnomAD v4: 4-39205952-A-ATGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205955_39205956insGGTGG , CM000666.2:g.39205955_39205956insGGTGG	GRCh38
NC_000004.11:g.39207575_39207576insGGTGG , CM000666.1:g.39207575_39207576insGGTGG	GRCh37
NC_000004.10:g.38883970_38883971insGGTGG	NCBI36
NG_031813.1:g.28552_28553insGGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.890+219_890+220insGGTGG MANE Select	ENSP00000382717.3:n.890+219_890+220insGGTGG
ENST00000399820.7:c.890+219_890+220insGGTGG	ENSP00000382717.3:n.890+219_890+220insGGTGG
ENST00000503697.5:c.*358+219_*358+220insGGTGG	ENSP00000423706.1:n.*358+219_*358+220insGGTGG
ENST00000506503.1:c.890+219_890+220insGGTGG	ENSP00000423491.1:n.890+219_890+220insGGTGG
ENST00000506869.5:c.*471+219_*471+220insGGTGG	ENSP00000424319.1:n.*471+219_*471+220insGGTGG
ENST00000511729.5:n.41-22603_41-22602insGGTGG
ENST00000512448.1:n.703_704insGGTGG
NM_025132.3:c.890+219_890+220insGGTGG	NP_079408.3:n.890+219_890+220insGGTGG
XM_011513724.1:c.890+219_890+220insGGTGG	XP_011512026.1:n.890+219_890+220insGGTGG
XM_011513725.1:c.824+219_824+220insGGTGG	XP_011512027.1:n.824+219_824+220insGGTGG
XM_011513726.1:c.410+219_410+220insGGTGG	XP_011512028.1:n.410+219_410+220insGGTGG
XM_011513727.1:c.410+219_410+220insGGTGG	XP_011512029.1:n.410+219_410+220insGGTGG
XM_011513728.1:c.410+219_410+220insGGTGG	XP_011512030.1:n.410+219_410+220insGGTGG
XM_011513729.1:c.890+219_890+220insGGTGG	XP_011512031.1:n.890+219_890+220insGGTGG
XR_925155.1:n.954+219_954+220insGGTGG
NM_001317924.1:c.410+219_410+220insGGTGG	NP_001304853.1:n.410+219_410+220insGGTGG
XM_011513725.2:c.824+219_824+220insGGTGG	XP_011512027.1:n.824+219_824+220insGGTGG
XM_011513726.3:c.410+219_410+220insGGTGG	XP_011512028.1:n.410+219_410+220insGGTGG
XM_017008501.1:c.410+219_410+220insGGTGG	XP_016863990.1:n.410+219_410+220insGGTGG
XR_001741306.1:n.954+219_954+220insGGTGG
XR_001741307.1:n.954+219_954+220insGGTGG
XR_001741308.1:n.954+219_954+220insGGTGG
XR_001741309.1:n.954+219_954+220insGGTGG
XR_001741310.1:n.954+219_954+220insGGTGG
XR_001741311.2:n.803+219_803+220insGGTGG
XR_001741312.1:n.954+219_954+220insGGTGG
NM_025132.4:c.890+219_890+220insGGTGG MANE Select	NP_079408.3:n.890+219_890+220insGGTGG
NM_001317924.2:c.410+219_410+220insGGTGG	NP_001304853.1:n.410+219_410+220insGGTGG