Canonical Allele Identifier: CA2761116417

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275035_39275036del , CM000666.2:g.39275035_39275036del	GRCh38
NC_000004.11:g.39276655_39276656del , CM000666.1:g.39276655_39276656del	GRCh37
NC_000004.10:g.38953050_38953051del	NCBI36
NG_031813.1:g.97632_97633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+77_3716+78del MANE Select	ENSP00000382717.3:n.3716+77_3716+78del
ENST00000399820.7:c.3716+77_3716+78del	ENSP00000382717.3:n.3716+77_3716+78del
ENST00000506869.5:c.*3297+77_*3297+78del	ENSP00000424319.1:n.*3297+77_*3297+78del
ENST00000512095.5:n.2791_2792del
ENST00000512534.5:n.2027+77_2027+78del
NM_025132.3:c.3716+77_3716+78del	NP_079408.3:n.3716+77_3716+78del
XM_011513724.1:c.3728+77_3728+78del	XP_011512026.1:n.3728+77_3728+78del
XM_011513725.1:c.3662+77_3662+78del	XP_011512027.1:n.3662+77_3662+78del
XM_011513726.1:c.3248+77_3248+78del	XP_011512028.1:n.3248+77_3248+78del
XM_011513727.1:c.3248+77_3248+78del	XP_011512029.1:n.3248+77_3248+78del
XM_011513728.1:c.3236+77_3236+78del	XP_011512030.1:n.3236+77_3236+78del
XR_925155.1:n.5426+77_5426+78del
NM_001317924.1:c.3236+77_3236+78del	NP_001304853.1:n.3236+77_3236+78del
XM_011513725.2:c.3662+77_3662+78del	XP_011512027.1:n.3662+77_3662+78del
XM_011513726.3:c.3248+77_3248+78del	XP_011512028.1:n.3248+77_3248+78del
XM_017008501.1:c.3236+77_3236+78del	XP_016863990.1:n.3236+77_3236+78del
XR_001741306.1:n.3792+77_3792+78del
XR_001741307.1:n.3780+77_3780+78del
XR_001741308.1:n.5426+77_5426+78del
XR_001741309.1:n.5414+77_5414+78del
XR_001741310.1:n.5414+77_5414+78del
XR_001741311.2:n.5263+77_5263+78del
NM_025132.4:c.3716+77_3716+78del MANE Select	NP_079408.3:n.3716+77_3716+78del
NM_001317924.2:c.3236+77_3236+78del	NP_001304853.1:n.3236+77_3236+78del