Canonical Allele Identifier: CA2670362545

Gene: WDR19

Linked Data

• gnomAD v4: 4-39275125-A-AACTACTGACCTCAAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39275125_39275126insACTACTGACCTCAAGT , CM000666.2:g.39275125_39275126insACTACTGACCTCAAGT	GRCh38
NC_000004.11:g.39276745_39276746insACTACTGACCTCAAGT , CM000666.1:g.39276745_39276746insACTACTGACCTCAAGT	GRCh37
NC_000004.10:g.38953140_38953141insACTACTGACCTCAAGT	NCBI36
NG_031813.1:g.97722_97723insACTACTGACCTCAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3716+167_3716+168insACTACTGACCTCAAGT MANE Select	ENSP00000382717.3:n.3716+167_3716+168insACTACTGACCTCAAGT
ENST00000399820.7:c.3716+167_3716+168insACTACTGACCTCAAGT	ENSP00000382717.3:n.3716+167_3716+168insACTACTGACCTCAAGT
ENST00000506869.5:c.*3297+167_*3297+168insACTACTGACCTCAAGT	ENSP00000424319.1:n.*3297+167_*3297+168insACTACTGACCTCAAGT
ENST00000512095.5:n.2881_2882insACTACTGACCTCAAGT
ENST00000512534.5:n.2027+167_2027+168insACTACTGACCTCAAGT
NM_025132.3:c.3716+167_3716+168insACTACTGACCTCAAGT	NP_079408.3:n.3716+167_3716+168insACTACTGACCTCAAGT
XM_011513724.1:c.3728+167_3728+168insACTACTGACCTCAAGT	XP_011512026.1:n.3728+167_3728+168insACTACTGACCTCAAGT
XM_011513725.1:c.3662+167_3662+168insACTACTGACCTCAAGT	XP_011512027.1:n.3662+167_3662+168insACTACTGACCTCAAGT
XM_011513726.1:c.3248+167_3248+168insACTACTGACCTCAAGT	XP_011512028.1:n.3248+167_3248+168insACTACTGACCTCAAGT
XM_011513727.1:c.3248+167_3248+168insACTACTGACCTCAAGT	XP_011512029.1:n.3248+167_3248+168insACTACTGACCTCAAGT
XM_011513728.1:c.3236+167_3236+168insACTACTGACCTCAAGT	XP_011512030.1:n.3236+167_3236+168insACTACTGACCTCAAGT
XR_925155.1:n.5426+167_5426+168insACTACTGACCTCAAGT
NM_001317924.1:c.3236+167_3236+168insACTACTGACCTCAAGT	NP_001304853.1:n.3236+167_3236+168insACTACTGACCTCAAGT
XM_011513725.2:c.3662+167_3662+168insACTACTGACCTCAAGT	XP_011512027.1:n.3662+167_3662+168insACTACTGACCTCAAGT
XM_011513726.3:c.3248+167_3248+168insACTACTGACCTCAAGT	XP_011512028.1:n.3248+167_3248+168insACTACTGACCTCAAGT
XM_017008501.1:c.3236+167_3236+168insACTACTGACCTCAAGT	XP_016863990.1:n.3236+167_3236+168insACTACTGACCTCAAGT
XR_001741306.1:n.3792+167_3792+168insACTACTGACCTCAAGT
XR_001741307.1:n.3780+167_3780+168insACTACTGACCTCAAGT
XR_001741308.1:n.5426+167_5426+168insACTACTGACCTCAAGT
XR_001741309.1:n.5414+167_5414+168insACTACTGACCTCAAGT
XR_001741310.1:n.5414+167_5414+168insACTACTGACCTCAAGT
XR_001741311.2:n.5263+167_5263+168insACTACTGACCTCAAGT
NM_025132.4:c.3716+167_3716+168insACTACTGACCTCAAGT MANE Select	NP_079408.3:n.3716+167_3716+168insACTACTGACCTCAAGT
NM_001317924.2:c.3236+167_3236+168insACTACTGACCTCAAGT	NP_001304853.1:n.3236+167_3236+168insACTACTGACCTCAAGT