Canonical Allele Identifier: CA2761116293

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274962_39274963del , CM000666.2:g.39274962_39274963del	GRCh38
NC_000004.11:g.39276582_39276583del , CM000666.1:g.39276582_39276583del	GRCh37
NC_000004.10:g.38952977_38952978del	NCBI36
NG_031813.1:g.97559_97560del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+4_3716+5del MANE Select	ENSP00000382717.3:n.3716+4_3716+5del
ENST00000399820.7:c.3716+4_3716+5del	ENSP00000382717.3:n.3716+4_3716+5del
ENST00000506869.5:c.*3297+4_*3297+5del	ENSP00000424319.1:n.*3297+4_*3297+5del
ENST00000512095.5:n.2718_2719del
ENST00000512534.5:n.2027+4_2027+5del
NM_025132.3:c.3716+4_3716+5del	NP_079408.3:n.3716+4_3716+5del
XM_011513724.1:c.3728+4_3728+5del	XP_011512026.1:n.3728+4_3728+5del
XM_011513725.1:c.3662+4_3662+5del	XP_011512027.1:n.3662+4_3662+5del
XM_011513726.1:c.3248+4_3248+5del	XP_011512028.1:n.3248+4_3248+5del
XM_011513727.1:c.3248+4_3248+5del	XP_011512029.1:n.3248+4_3248+5del
XM_011513728.1:c.3236+4_3236+5del	XP_011512030.1:n.3236+4_3236+5del
XR_925155.1:n.5426+4_5426+5del
NM_001317924.1:c.3236+4_3236+5del	NP_001304853.1:n.3236+4_3236+5del
XM_011513725.2:c.3662+4_3662+5del	XP_011512027.1:n.3662+4_3662+5del
XM_011513726.3:c.3248+4_3248+5del	XP_011512028.1:n.3248+4_3248+5del
XM_017008501.1:c.3236+4_3236+5del	XP_016863990.1:n.3236+4_3236+5del
XR_001741306.1:n.3792+4_3792+5del
XR_001741307.1:n.3780+4_3780+5del
XR_001741308.1:n.5426+4_5426+5del
XR_001741309.1:n.5414+4_5414+5del
XR_001741310.1:n.5414+4_5414+5del
XR_001741311.2:n.5263+4_5263+5del
NM_025132.4:c.3716+4_3716+5del MANE Select	NP_079408.3:n.3716+4_3716+5del
NM_001317924.2:c.3236+4_3236+5del	NP_001304853.1:n.3236+4_3236+5del