Canonical Allele Identifier: CA2534081337

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275188_39275190dup , CM000666.2:g.39275188_39275190dup	GRCh38
NC_000004.11:g.39276808_39276810dup , CM000666.1:g.39276808_39276810dup	GRCh37
NC_000004.10:g.38953203_38953205dup	NCBI36
NG_031813.1:g.97785_97787dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+230_3716+232dup MANE Select	ENSP00000382717.3:n.3716+230_3716+232dup
ENST00000399820.7:c.3716+230_3716+232dup	ENSP00000382717.3:n.3716+230_3716+232dup
ENST00000506869.5:c.*3297+230_*3297+232dup	ENSP00000424319.1:n.*3297+230_*3297+232dup
ENST00000512095.5:n.2944_2946dup
ENST00000512534.5:n.2027+230_2027+232dup
NM_025132.3:c.3716+230_3716+232dup	NP_079408.3:n.3716+230_3716+232dup
XM_011513724.1:c.3728+230_3728+232dup	XP_011512026.1:n.3728+230_3728+232dup
XM_011513725.1:c.3662+230_3662+232dup	XP_011512027.1:n.3662+230_3662+232dup
XM_011513726.1:c.3248+230_3248+232dup	XP_011512028.1:n.3248+230_3248+232dup
XM_011513727.1:c.3248+230_3248+232dup	XP_011512029.1:n.3248+230_3248+232dup
XM_011513728.1:c.3236+230_3236+232dup	XP_011512030.1:n.3236+230_3236+232dup
XR_925155.1:n.5426+230_5426+232dup
NM_001317924.1:c.3236+230_3236+232dup	NP_001304853.1:n.3236+230_3236+232dup
XM_011513725.2:c.3662+230_3662+232dup	XP_011512027.1:n.3662+230_3662+232dup
XM_011513726.3:c.3248+230_3248+232dup	XP_011512028.1:n.3248+230_3248+232dup
XM_017008501.1:c.3236+230_3236+232dup	XP_016863990.1:n.3236+230_3236+232dup
XR_001741306.1:n.3792+230_3792+232dup
XR_001741307.1:n.3780+230_3780+232dup
XR_001741308.1:n.5426+230_5426+232dup
XR_001741309.1:n.5414+230_5414+232dup
XR_001741310.1:n.5414+230_5414+232dup
XR_001741311.2:n.5263+230_5263+232dup
NM_025132.4:c.3716+230_3716+232dup MANE Select	NP_079408.3:n.3716+230_3716+232dup
NM_001317924.2:c.3236+230_3236+232dup	NP_001304853.1:n.3236+230_3236+232dup