Canonical Allele Identifier: CA2761116329

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274981_39274982insAGA , CM000666.2:g.39274981_39274982insAGA	GRCh38
NC_000004.11:g.39276601_39276602insAGA , CM000666.1:g.39276601_39276602insAGA	GRCh37
NC_000004.10:g.38952996_38952997insAGA	NCBI36
NG_031813.1:g.97578_97579insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+23_3716+24insAGA MANE Select	ENSP00000382717.3:n.3716+23_3716+24insAGA
ENST00000399820.7:c.3716+23_3716+24insAGA	ENSP00000382717.3:n.3716+23_3716+24insAGA
ENST00000506869.5:c.*3297+23_*3297+24insAGA	ENSP00000424319.1:n.*3297+23_*3297+24insAGA
ENST00000512095.5:n.2737_2738insAGA
ENST00000512534.5:n.2027+23_2027+24insAGA
NM_025132.3:c.3716+23_3716+24insAGA	NP_079408.3:n.3716+23_3716+24insAGA
XM_011513724.1:c.3728+23_3728+24insAGA	XP_011512026.1:n.3728+23_3728+24insAGA
XM_011513725.1:c.3662+23_3662+24insAGA	XP_011512027.1:n.3662+23_3662+24insAGA
XM_011513726.1:c.3248+23_3248+24insAGA	XP_011512028.1:n.3248+23_3248+24insAGA
XM_011513727.1:c.3248+23_3248+24insAGA	XP_011512029.1:n.3248+23_3248+24insAGA
XM_011513728.1:c.3236+23_3236+24insAGA	XP_011512030.1:n.3236+23_3236+24insAGA
XR_925155.1:n.5426+23_5426+24insAGA
NM_001317924.1:c.3236+23_3236+24insAGA	NP_001304853.1:n.3236+23_3236+24insAGA
XM_011513725.2:c.3662+23_3662+24insAGA	XP_011512027.1:n.3662+23_3662+24insAGA
XM_011513726.3:c.3248+23_3248+24insAGA	XP_011512028.1:n.3248+23_3248+24insAGA
XM_017008501.1:c.3236+23_3236+24insAGA	XP_016863990.1:n.3236+23_3236+24insAGA
XR_001741306.1:n.3792+23_3792+24insAGA
XR_001741307.1:n.3780+23_3780+24insAGA
XR_001741308.1:n.5426+23_5426+24insAGA
XR_001741309.1:n.5414+23_5414+24insAGA
XR_001741310.1:n.5414+23_5414+24insAGA
XR_001741311.2:n.5263+23_5263+24insAGA
NM_025132.4:c.3716+23_3716+24insAGA MANE Select	NP_079408.3:n.3716+23_3716+24insAGA
NM_001317924.2:c.3236+23_3236+24insAGA	NP_001304853.1:n.3236+23_3236+24insAGA