Canonical Allele Identifier: CA645539491

Gene: WDR19

Linked Data

• COSMIC: COSM4740880

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205174del , CM000666.2:g.39205174del	GRCh38
NC_000004.11:g.39206794del , CM000666.1:g.39206794del	GRCh37
NC_000004.10:g.38883189del	NCBI36
NG_031813.1:g.27771del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.624del MANE Select	ENSP00000382717.3:p.Thr210LeufsTer5
ENST00000399820.7:c.624del	ENSP00000382717.3:p.Thr210LeufsTer5
ENST00000503697.5:c.*92del	ENSP00000423706.1:n.*92del
ENST00000505055.5:c.*205del	ENSP00000425949.1:n.*205del
ENST00000506503.1:c.624del	ENSP00000423491.1:p.Thr210LeufsTer5
ENST00000506869.5:c.*205del	ENSP00000424319.1:n.*205del
ENST00000511729.5:n.40+22611del
ENST00000512448.1:n.218del
NM_025132.3:c.624del	NP_079408.3:p.Thr210LeufsTer5
XM_011513724.1:c.624del	XP_011512026.1:p.Thr210LeufsTer5
XM_011513725.1:c.558del	XP_011512027.1:p.Thr188LeufsTer5
XM_011513726.1:c.144del	XP_011512028.1:p.Thr50LeufsTer5
XM_011513727.1:c.144del	XP_011512029.1:p.Thr50LeufsTer5
XM_011513728.1:c.144del	XP_011512030.1:p.Thr50LeufsTer5
XM_011513729.1:c.624del	XP_011512031.1:p.Thr210LeufsTer5
XR_925155.1:n.688del
NM_001317924.1:c.144del	NP_001304853.1:p.Thr50LeufsTer5
XM_011513725.2:c.558del	XP_011512027.1:p.Thr188LeufsTer5
XM_011513726.3:c.144del	XP_011512028.1:p.Thr50LeufsTer5
XM_017008501.1:c.144del	XP_016863990.1:p.Thr50LeufsTer5
XR_001741306.1:n.688del
XR_001741307.1:n.688del
XR_001741308.1:n.688del
XR_001741309.1:n.688del
XR_001741310.1:n.688del
XR_001741311.2:n.537del
XR_001741312.1:n.688del
NM_025132.4:c.624del MANE Select	NP_079408.3:p.Thr210LeufsTer5
NM_001317924.2:c.144del	NP_001304853.1:p.Thr50LeufsTer5