Canonical Allele Identifier: CA2761116438

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275071_39275075del , CM000666.2:g.39275071_39275075del	GRCh38
NC_000004.11:g.39276691_39276695del , CM000666.1:g.39276691_39276695del	GRCh37
NC_000004.10:g.38953086_38953090del	NCBI36
NG_031813.1:g.97668_97672del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+113_3716+117del MANE Select	ENSP00000382717.3:n.3716+113_3716+117del
ENST00000399820.7:c.3716+113_3716+117del	ENSP00000382717.3:n.3716+113_3716+117del
ENST00000506869.5:c.*3297+113_*3297+117del	ENSP00000424319.1:n.*3297+113_*3297+117del
ENST00000512095.5:n.2827_2831del
ENST00000512534.5:n.2027+113_2027+117del
NM_025132.3:c.3716+113_3716+117del	NP_079408.3:n.3716+113_3716+117del
XM_011513724.1:c.3728+113_3728+117del	XP_011512026.1:n.3728+113_3728+117del
XM_011513725.1:c.3662+113_3662+117del	XP_011512027.1:n.3662+113_3662+117del
XM_011513726.1:c.3248+113_3248+117del	XP_011512028.1:n.3248+113_3248+117del
XM_011513727.1:c.3248+113_3248+117del	XP_011512029.1:n.3248+113_3248+117del
XM_011513728.1:c.3236+113_3236+117del	XP_011512030.1:n.3236+113_3236+117del
XR_925155.1:n.5426+113_5426+117del
NM_001317924.1:c.3236+113_3236+117del	NP_001304853.1:n.3236+113_3236+117del
XM_011513725.2:c.3662+113_3662+117del	XP_011512027.1:n.3662+113_3662+117del
XM_011513726.3:c.3248+113_3248+117del	XP_011512028.1:n.3248+113_3248+117del
XM_017008501.1:c.3236+113_3236+117del	XP_016863990.1:n.3236+113_3236+117del
XR_001741306.1:n.3792+113_3792+117del
XR_001741307.1:n.3780+113_3780+117del
XR_001741308.1:n.5426+113_5426+117del
XR_001741309.1:n.5414+113_5414+117del
XR_001741310.1:n.5414+113_5414+117del
XR_001741311.2:n.5263+113_5263+117del
NM_025132.4:c.3716+113_3716+117del MANE Select	NP_079408.3:n.3716+113_3716+117del
NM_001317924.2:c.3236+113_3236+117del	NP_001304853.1:n.3236+113_3236+117del