Canonical Allele Identifier: CA2761116415

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275033_39275034del , CM000666.2:g.39275033_39275034del	GRCh38
NC_000004.11:g.39276653_39276654del , CM000666.1:g.39276653_39276654del	GRCh37
NC_000004.10:g.38953048_38953049del	NCBI36
NG_031813.1:g.97630_97631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+75_3716+76del MANE Select	ENSP00000382717.3:n.3716+75_3716+76del
ENST00000399820.7:c.3716+75_3716+76del	ENSP00000382717.3:n.3716+75_3716+76del
ENST00000506869.5:c.*3297+75_*3297+76del	ENSP00000424319.1:n.*3297+75_*3297+76del
ENST00000512095.5:n.2789_2790del
ENST00000512534.5:n.2027+75_2027+76del
NM_025132.3:c.3716+75_3716+76del	NP_079408.3:n.3716+75_3716+76del
XM_011513724.1:c.3728+75_3728+76del	XP_011512026.1:n.3728+75_3728+76del
XM_011513725.1:c.3662+75_3662+76del	XP_011512027.1:n.3662+75_3662+76del
XM_011513726.1:c.3248+75_3248+76del	XP_011512028.1:n.3248+75_3248+76del
XM_011513727.1:c.3248+75_3248+76del	XP_011512029.1:n.3248+75_3248+76del
XM_011513728.1:c.3236+75_3236+76del	XP_011512030.1:n.3236+75_3236+76del
XR_925155.1:n.5426+75_5426+76del
NM_001317924.1:c.3236+75_3236+76del	NP_001304853.1:n.3236+75_3236+76del
XM_011513725.2:c.3662+75_3662+76del	XP_011512027.1:n.3662+75_3662+76del
XM_011513726.3:c.3248+75_3248+76del	XP_011512028.1:n.3248+75_3248+76del
XM_017008501.1:c.3236+75_3236+76del	XP_016863990.1:n.3236+75_3236+76del
XR_001741306.1:n.3792+75_3792+76del
XR_001741307.1:n.3780+75_3780+76del
XR_001741308.1:n.5426+75_5426+76del
XR_001741309.1:n.5414+75_5414+76del
XR_001741310.1:n.5414+75_5414+76del
XR_001741311.2:n.5263+75_5263+76del
NM_025132.4:c.3716+75_3716+76del MANE Select	NP_079408.3:n.3716+75_3716+76del
NM_001317924.2:c.3236+75_3236+76del	NP_001304853.1:n.3236+75_3236+76del