Canonical Allele Identifier: CA2670356242

Gene: WDR19

Linked Data

• gnomAD v4: 4-39205321-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205321_39205322insAT , CM000666.2:g.39205321_39205322insAT	GRCh38
NC_000004.11:g.39206941_39206942insAT , CM000666.1:g.39206941_39206942insAT	GRCh37
NC_000004.10:g.38883336_38883337insAT	NCBI36
NG_031813.1:g.27918_27919insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.716+55_716+56insAT MANE Select	ENSP00000382717.3:n.716+55_716+56insAT
ENST00000399820.7:c.716+55_716+56insAT	ENSP00000382717.3:n.716+55_716+56insAT
ENST00000503697.5:c.*184+55_*184+56insAT	ENSP00000423706.1:n.*184+55_*184+56insAT
ENST00000505055.5:c.*297+55_*297+56insAT	ENSP00000425949.1:n.*297+55_*297+56insAT
ENST00000506503.1:c.716+55_716+56insAT	ENSP00000423491.1:n.716+55_716+56insAT
ENST00000506869.5:c.*297+55_*297+56insAT	ENSP00000424319.1:n.*297+55_*297+56insAT
ENST00000511729.5:n.40+22758_40+22759insAT
ENST00000512448.1:n.310+55_310+56insAT
NM_025132.3:c.716+55_716+56insAT	NP_079408.3:n.716+55_716+56insAT
XM_011513724.1:c.716+55_716+56insAT	XP_011512026.1:n.716+55_716+56insAT
XM_011513725.1:c.650+55_650+56insAT	XP_011512027.1:n.650+55_650+56insAT
XM_011513726.1:c.236+55_236+56insAT	XP_011512028.1:n.236+55_236+56insAT
XM_011513727.1:c.236+55_236+56insAT	XP_011512029.1:n.236+55_236+56insAT
XM_011513728.1:c.236+55_236+56insAT	XP_011512030.1:n.236+55_236+56insAT
XM_011513729.1:c.716+55_716+56insAT	XP_011512031.1:n.716+55_716+56insAT
XR_925155.1:n.780+55_780+56insAT
NM_001317924.1:c.236+55_236+56insAT	NP_001304853.1:n.236+55_236+56insAT
XM_011513725.2:c.650+55_650+56insAT	XP_011512027.1:n.650+55_650+56insAT
XM_011513726.3:c.236+55_236+56insAT	XP_011512028.1:n.236+55_236+56insAT
XM_017008501.1:c.236+55_236+56insAT	XP_016863990.1:n.236+55_236+56insAT
XR_001741306.1:n.780+55_780+56insAT
XR_001741307.1:n.780+55_780+56insAT
XR_001741308.1:n.780+55_780+56insAT
XR_001741309.1:n.780+55_780+56insAT
XR_001741310.1:n.780+55_780+56insAT
XR_001741311.2:n.629+55_629+56insAT
XR_001741312.1:n.780+55_780+56insAT
NM_025132.4:c.716+55_716+56insAT MANE Select	NP_079408.3:n.716+55_716+56insAT
NM_001317924.2:c.236+55_236+56insAT	NP_001304853.1:n.236+55_236+56insAT