Canonical Allele Identifier: CA2521824275

Gene: WDR19

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39274959_39274960insA , CM000666.2:g.39274959_39274960insA	GRCh38
NC_000004.11:g.39276579_39276580insA , CM000666.1:g.39276579_39276580insA	GRCh37
NC_000004.10:g.38952974_38952975insA	NCBI36
NG_031813.1:g.97556_97557insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+1_3716+2insA MANE Select	ENSP00000382717.3:n.3716+1_3716+2insA
ENST00000399820.7:c.3716+1_3716+2insA	ENSP00000382717.3:n.3716+1_3716+2insA
ENST00000506869.5:c.*3297+1_*3297+2insA	ENSP00000424319.1:n.*3297+1_*3297+2insA
ENST00000512095.5:n.2715_2716insA
ENST00000512534.5:n.2027+1_2027+2insA
NM_025132.3:c.3716+1_3716+2insA	NP_079408.3:n.3716+1_3716+2insA
XM_011513724.1:c.3728+1_3728+2insA	XP_011512026.1:n.3728+1_3728+2insA
XM_011513725.1:c.3662+1_3662+2insA	XP_011512027.1:n.3662+1_3662+2insA
XM_011513726.1:c.3248+1_3248+2insA	XP_011512028.1:n.3248+1_3248+2insA
XM_011513727.1:c.3248+1_3248+2insA	XP_011512029.1:n.3248+1_3248+2insA
XM_011513728.1:c.3236+1_3236+2insA	XP_011512030.1:n.3236+1_3236+2insA
XR_925155.1:n.5426+1_5426+2insA
NM_001317924.1:c.3236+1_3236+2insA	NP_001304853.1:n.3236+1_3236+2insA
XM_011513725.2:c.3662+1_3662+2insA	XP_011512027.1:n.3662+1_3662+2insA
XM_011513726.3:c.3248+1_3248+2insA	XP_011512028.1:n.3248+1_3248+2insA
XM_017008501.1:c.3236+1_3236+2insA	XP_016863990.1:n.3236+1_3236+2insA
XR_001741306.1:n.3792+1_3792+2insA
XR_001741307.1:n.3780+1_3780+2insA
XR_001741308.1:n.5426+1_5426+2insA
XR_001741309.1:n.5414+1_5414+2insA
XR_001741310.1:n.5414+1_5414+2insA
XR_001741311.2:n.5263+1_5263+2insA
NM_025132.4:c.3716+1_3716+2insA MANE Select	NP_079408.3:n.3716+1_3716+2insA
NM_001317924.2:c.3236+1_3236+2insA	NP_001304853.1:n.3236+1_3236+2insA