Canonical Allele Identifier: CA2670362457

Gene: WDR19

Linked Data

• gnomAD v4: 4-39275027-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275031_39275032del , CM000666.2:g.39275031_39275032del	GRCh38
NC_000004.11:g.39276651_39276652del , CM000666.1:g.39276651_39276652del	GRCh37
NC_000004.10:g.38953046_38953047del	NCBI36
NG_031813.1:g.97628_97629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+73_3716+74del MANE Select	ENSP00000382717.3:n.3716+73_3716+74del
ENST00000399820.7:c.3716+73_3716+74del	ENSP00000382717.3:n.3716+73_3716+74del
ENST00000506869.5:c.*3297+73_*3297+74del	ENSP00000424319.1:n.*3297+73_*3297+74del
ENST00000512095.5:n.2787_2788del
ENST00000512534.5:n.2027+73_2027+74del
NM_025132.3:c.3716+73_3716+74del	NP_079408.3:n.3716+73_3716+74del
XM_011513724.1:c.3728+73_3728+74del	XP_011512026.1:n.3728+73_3728+74del
XM_011513725.1:c.3662+73_3662+74del	XP_011512027.1:n.3662+73_3662+74del
XM_011513726.1:c.3248+73_3248+74del	XP_011512028.1:n.3248+73_3248+74del
XM_011513727.1:c.3248+73_3248+74del	XP_011512029.1:n.3248+73_3248+74del
XM_011513728.1:c.3236+73_3236+74del	XP_011512030.1:n.3236+73_3236+74del
XR_925155.1:n.5426+73_5426+74del
NM_001317924.1:c.3236+73_3236+74del	NP_001304853.1:n.3236+73_3236+74del
XM_011513725.2:c.3662+73_3662+74del	XP_011512027.1:n.3662+73_3662+74del
XM_011513726.3:c.3248+73_3248+74del	XP_011512028.1:n.3248+73_3248+74del
XM_017008501.1:c.3236+73_3236+74del	XP_016863990.1:n.3236+73_3236+74del
XR_001741306.1:n.3792+73_3792+74del
XR_001741307.1:n.3780+73_3780+74del
XR_001741308.1:n.5426+73_5426+74del
XR_001741309.1:n.5414+73_5414+74del
XR_001741310.1:n.5414+73_5414+74del
XR_001741311.2:n.5263+73_5263+74del
NM_025132.4:c.3716+73_3716+74del MANE Select	NP_079408.3:n.3716+73_3716+74del
NM_001317924.2:c.3236+73_3236+74del	NP_001304853.1:n.3236+73_3236+74del