Canonical Allele Identifier: CA2815519191
Gene: KIZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.21136510_21136512del , CM000682.2:g.21136510_21136512del GRCh38
NC_000020.10:g.21117151_21117153del , CM000682.1:g.21117151_21117153del GRCh37
NC_000020.9:g.21065151_21065153del NCBI36
NG_033122.1:g.15528_15530del
NG_033122.2:g.15531_15533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000619189.5:c.273_275del MANE Select ENSP00000479542.1:p.Val92del
ENST00000611685.4:c.167-9055_167-9053del
ENST00000616848.4:c.6+4351_6+4353del ENSP00000480612.1:n.6+4351_6+4353del
ENST00000619189.4:c.273_275del ENSP00000479542.1:p.Val92del
ENST00000619574.4:c.169-9055_169-9053del ENSP00000484706.1:n.169-9055_169-9053del
ENST00000620553.2:n.329_331del
ENST00000620891.4:c.6+4351_6+4353del ENSP00000478019.1:n.6+4351_6+4353del
NM_001163022.1:c.6+4351_6+4353del NP_001156494.1:n.6+4351_6+4353del
NM_001163023.1:c.6+4351_6+4353del NP_001156495.1:n.6+4351_6+4353del
NM_001276389.1:c.169-9055_169-9053del NP_001263318.1:n.169-9055_169-9053del
NM_018474.4:c.273_275del NP_060944.3:p.Val92del
XM_011529296.1:c.273_275del XP_011527598.1:p.Val92del
XM_011529297.1:c.273_275del XP_011527599.1:p.Val92del
XM_011529298.1:c.273_275del XP_011527600.1:p.Val92del
XM_011529299.1:c.6+4351_6+4353del XP_011527601.1:n.6+4351_6+4353del
XR_937105.1:n.397_399del
NM_001163022.2:c.6+4351_6+4353del NP_001156494.1:n.6+4351_6+4353del
NM_001163023.2:c.6+4351_6+4353del NP_001156495.1:n.6+4351_6+4353del
NM_001276389.2:c.169-9055_169-9053del NP_001263318.1:n.169-9055_169-9053del
NM_001352434.1:c.273_275del NP_001339363.1:p.Val92del
NM_001352435.1:c.6+4351_6+4353del NP_001339364.1:n.6+4351_6+4353del
NM_001352436.1:c.-114_-112del NP_001339365.1:n.-114_-112del
NM_018474.5:c.273_275del NP_060944.3:p.Val92del
XM_011529296.3:c.273_275del XP_011527598.1:p.Val92del
XM_011529297.3:c.273_275del XP_011527599.1:p.Val92del
XM_011529299.3:c.6+4351_6+4353del XP_011527601.1:n.6+4351_6+4353del
XM_017027951.2:c.-114_-112del XP_016883440.1:n.-114_-112del
XM_017027952.2:c.6+4351_6+4353del XP_016883441.1:n.6+4351_6+4353del
XR_001754334.2:n.339_341del
XR_937105.3:n.339_341del
NM_018474.6:c.273_275del MANE Select NP_060944.3:p.Val92del
NM_001163022.3:c.6+4351_6+4353del NP_001156494.1:n.6+4351_6+4353del
NM_001163023.3:c.6+4351_6+4353del NP_001156495.1:n.6+4351_6+4353del
NM_001352434.2:c.273_275del NP_001339363.1:p.Val92del
NM_001352435.2:c.6+4351_6+4353del NP_001339364.1:n.6+4351_6+4353del
NM_001352436.2:c.-114_-112del NP_001339365.1:n.-114_-112del