Canonical Allele Identifier: CA2761116346

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274988_39274989insG , CM000666.2:g.39274988_39274989insG	GRCh38
NC_000004.11:g.39276608_39276609insG , CM000666.1:g.39276608_39276609insG	GRCh37
NC_000004.10:g.38953003_38953004insG	NCBI36
NG_031813.1:g.97585_97586insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+30_3716+31insG MANE Select	ENSP00000382717.3:n.3716+30_3716+31insG
ENST00000399820.7:c.3716+30_3716+31insG	ENSP00000382717.3:n.3716+30_3716+31insG
ENST00000506869.5:c.*3297+30_*3297+31insG	ENSP00000424319.1:n.*3297+30_*3297+31insG
ENST00000512095.5:n.2744_2745insG
ENST00000512534.5:n.2027+30_2027+31insG
NM_025132.3:c.3716+30_3716+31insG	NP_079408.3:n.3716+30_3716+31insG
XM_011513724.1:c.3728+30_3728+31insG	XP_011512026.1:n.3728+30_3728+31insG
XM_011513725.1:c.3662+30_3662+31insG	XP_011512027.1:n.3662+30_3662+31insG
XM_011513726.1:c.3248+30_3248+31insG	XP_011512028.1:n.3248+30_3248+31insG
XM_011513727.1:c.3248+30_3248+31insG	XP_011512029.1:n.3248+30_3248+31insG
XM_011513728.1:c.3236+30_3236+31insG	XP_011512030.1:n.3236+30_3236+31insG
XR_925155.1:n.5426+30_5426+31insG
NM_001317924.1:c.3236+30_3236+31insG	NP_001304853.1:n.3236+30_3236+31insG
XM_011513725.2:c.3662+30_3662+31insG	XP_011512027.1:n.3662+30_3662+31insG
XM_011513726.3:c.3248+30_3248+31insG	XP_011512028.1:n.3248+30_3248+31insG
XM_017008501.1:c.3236+30_3236+31insG	XP_016863990.1:n.3236+30_3236+31insG
XR_001741306.1:n.3792+30_3792+31insG
XR_001741307.1:n.3780+30_3780+31insG
XR_001741308.1:n.5426+30_5426+31insG
XR_001741309.1:n.5414+30_5414+31insG
XR_001741310.1:n.5414+30_5414+31insG
XR_001741311.2:n.5263+30_5263+31insG
NM_025132.4:c.3716+30_3716+31insG MANE Select	NP_079408.3:n.3716+30_3716+31insG
NM_001317924.2:c.3236+30_3236+31insG	NP_001304853.1:n.3236+30_3236+31insG