Canonical Allele Identifier: CA2815519257
Gene: KIZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.21136635_21136636insACA , CM000682.2:g.21136635_21136636insACA GRCh38
NC_000020.10:g.21117276_21117277insACA , CM000682.1:g.21117276_21117277insACA GRCh37
NC_000020.9:g.21065276_21065277insACA NCBI36
NG_033122.1:g.15653_15654insACA
NG_033122.2:g.15656_15657insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000619189.5:c.315+83_315+84insACA MANE Select ENSP00000479542.1:n.315+83_315+84insACA
ENST00000611685.4:c.167-8930_167-8929insACA
ENST00000616848.4:c.6+4476_6+4477insACA ENSP00000480612.1:n.6+4476_6+4477insACA
ENST00000619189.4:c.315+83_315+84insACA ENSP00000479542.1:n.315+83_315+84insACA
ENST00000619574.4:c.169-8930_169-8929insACA ENSP00000484706.1:n.169-8930_169-8929insACA
ENST00000620553.2:n.371+83_371+84insACA
ENST00000620891.4:c.6+4476_6+4477insACA ENSP00000478019.1:n.6+4476_6+4477insACA
NM_001163022.1:c.6+4476_6+4477insACA NP_001156494.1:n.6+4476_6+4477insACA
NM_001163023.1:c.6+4476_6+4477insACA NP_001156495.1:n.6+4476_6+4477insACA
NM_001276389.1:c.169-8930_169-8929insACA NP_001263318.1:n.169-8930_169-8929insACA
NM_018474.4:c.315+83_315+84insACA NP_060944.3:n.315+83_315+84insACA
XM_011529296.1:c.315+83_315+84insACA XP_011527598.1:n.315+83_315+84insACA
XM_011529297.1:c.315+83_315+84insACA XP_011527599.1:n.315+83_315+84insACA
XM_011529298.1:c.315+83_315+84insACA XP_011527600.1:n.315+83_315+84insACA
XM_011529299.1:c.6+4476_6+4477insACA XP_011527601.1:n.6+4476_6+4477insACA
XR_937105.1:n.439+83_439+84insACA
NM_001163022.2:c.6+4476_6+4477insACA NP_001156494.1:n.6+4476_6+4477insACA
NM_001163023.2:c.6+4476_6+4477insACA NP_001156495.1:n.6+4476_6+4477insACA
NM_001276389.2:c.169-8930_169-8929insACA NP_001263318.1:n.169-8930_169-8929insACA
NM_001352434.1:c.315+83_315+84insACA NP_001339363.1:n.315+83_315+84insACA
NM_001352435.1:c.6+4476_6+4477insACA NP_001339364.1:n.6+4476_6+4477insACA
NM_001352436.1:c.-72+83_-72+84insACA NP_001339365.1:n.-72+83_-72+84insACA
NM_018474.5:c.315+83_315+84insACA NP_060944.3:n.315+83_315+84insACA
XM_011529296.3:c.315+83_315+84insACA XP_011527598.1:n.315+83_315+84insACA
XM_011529297.3:c.315+83_315+84insACA XP_011527599.1:n.315+83_315+84insACA
XM_011529299.3:c.6+4476_6+4477insACA XP_011527601.1:n.6+4476_6+4477insACA
XM_017027951.2:c.-72+83_-72+84insACA XP_016883440.1:n.-72+83_-72+84insACA
XM_017027952.2:c.6+4476_6+4477insACA XP_016883441.1:n.6+4476_6+4477insACA
XR_001754334.2:n.381+83_381+84insACA
XR_937105.3:n.381+83_381+84insACA
NM_018474.6:c.315+83_315+84insACA MANE Select NP_060944.3:n.315+83_315+84insACA
NM_001163022.3:c.6+4476_6+4477insACA NP_001156494.1:n.6+4476_6+4477insACA
NM_001163023.3:c.6+4476_6+4477insACA NP_001156495.1:n.6+4476_6+4477insACA
NM_001352434.2:c.315+83_315+84insACA NP_001339363.1:n.315+83_315+84insACA
NM_001352435.2:c.6+4476_6+4477insACA NP_001339364.1:n.6+4476_6+4477insACA
NM_001352436.2:c.-72+83_-72+84insACA NP_001339365.1:n.-72+83_-72+84insACA