Canonical Allele Identifier: CA2354742709
Gene: KIZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.21136223_21136227delinsTTCTC , CM000682.2:g.21136223_21136227delinsTTCTC GRCh38
NC_000020.10:g.21116864_21116868delinsTTCTC , CM000682.1:g.21116864_21116868delinsTTCTC GRCh37
NC_000020.9:g.21064864_21064868delinsTTCTC NCBI36
NG_033122.1:g.15241_15245delinsTTCTC
NG_033122.2:g.15244_15248delinsTTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000619189.5:c.153-167_153-163delinsTTCTC MANE Select ENSP00000479542.1:n.153-167_153-163delinsTTCTC
ENST00000611685.4:c.167-9342_167-9338delinsTTCTC
ENST00000612654.1:c.*61-167_*61-163delinsTTCTC ENSP00000480859.1:n.*61-167_*61-163delinsTTCTC
ENST00000616848.4:c.6+4064_6+4068delinsTTCTC ENSP00000480612.1:n.6+4064_6+4068delinsTTCTC
ENST00000619189.4:c.153-167_153-163delinsTTCTC ENSP00000479542.1:n.153-167_153-163delinsTTCTC
ENST00000619574.4:c.169-9342_169-9338delinsTTCTC ENSP00000484706.1:n.169-9342_169-9338delinsTTCTC
ENST00000620553.2:n.209-167_209-163delinsTTCTC
ENST00000620891.4:c.6+4064_6+4068delinsTTCTC ENSP00000478019.1:n.6+4064_6+4068delinsTTCTC
NM_001163022.1:c.6+4064_6+4068delinsTTCTC NP_001156494.1:n.6+4064_6+4068delinsTTCTC
NM_001163023.1:c.6+4064_6+4068delinsTTCTC NP_001156495.1:n.6+4064_6+4068delinsTTCTC
NM_001276389.1:c.169-9342_169-9338delinsTTCTC NP_001263318.1:n.169-9342_169-9338delinsTTCTC
NM_018474.4:c.153-167_153-163delinsTTCTC NP_060944.3:n.153-167_153-163delinsTTCTC
XM_011529296.1:c.153-167_153-163delinsTTCTC XP_011527598.1:n.153-167_153-163delinsTTCTC
XM_011529297.1:c.153-167_153-163delinsTTCTC XP_011527599.1:n.153-167_153-163delinsTTCTC
XM_011529298.1:c.153-167_153-163delinsTTCTC XP_011527600.1:n.153-167_153-163delinsTTCTC
XM_011529299.1:c.6+4064_6+4068delinsTTCTC XP_011527601.1:n.6+4064_6+4068delinsTTCTC
XR_937105.1:n.277-167_277-163delinsTTCTC
NM_001163022.2:c.6+4064_6+4068delinsTTCTC NP_001156494.1:n.6+4064_6+4068delinsTTCTC
NM_001163023.2:c.6+4064_6+4068delinsTTCTC NP_001156495.1:n.6+4064_6+4068delinsTTCTC
NM_001276389.2:c.169-9342_169-9338delinsTTCTC NP_001263318.1:n.169-9342_169-9338delinsTTCTC
NM_001352434.1:c.153-167_153-163delinsTTCTC NP_001339363.1:n.153-167_153-163delinsTTCTC
NM_001352435.1:c.6+4064_6+4068delinsTTCTC NP_001339364.1:n.6+4064_6+4068delinsTTCTC
NM_001352436.1:c.-234-167_-234-163delinsTTCTC NP_001339365.1:n.-234-167_-234-163delinsTTCTC
NM_018474.5:c.153-167_153-163delinsTTCTC NP_060944.3:n.153-167_153-163delinsTTCTC
XM_011529296.3:c.153-167_153-163delinsTTCTC XP_011527598.1:n.153-167_153-163delinsTTCTC
XM_011529297.3:c.153-167_153-163delinsTTCTC XP_011527599.1:n.153-167_153-163delinsTTCTC
XM_011529299.3:c.6+4064_6+4068delinsTTCTC XP_011527601.1:n.6+4064_6+4068delinsTTCTC
XM_017027951.2:c.-234-167_-234-163delinsTTCTC XP_016883440.1:n.-234-167_-234-163delinsTTCTC
XM_017027952.2:c.6+4064_6+4068delinsTTCTC XP_016883441.1:n.6+4064_6+4068delinsTTCTC
XR_001754334.2:n.219-167_219-163delinsTTCTC
XR_937105.3:n.219-167_219-163delinsTTCTC
NM_018474.6:c.153-167_153-163delinsTTCTC MANE Select NP_060944.3:n.153-167_153-163delinsTTCTC
NM_001163022.3:c.6+4064_6+4068delinsTTCTC NP_001156494.1:n.6+4064_6+4068delinsTTCTC
NM_001163023.3:c.6+4064_6+4068delinsTTCTC NP_001156495.1:n.6+4064_6+4068delinsTTCTC
NM_001352434.2:c.153-167_153-163delinsTTCTC NP_001339363.1:n.153-167_153-163delinsTTCTC
NM_001352435.2:c.6+4064_6+4068delinsTTCTC NP_001339364.1:n.6+4064_6+4068delinsTTCTC
NM_001352436.2:c.-234-167_-234-163delinsTTCTC NP_001339365.1:n.-234-167_-234-163delinsTTCTC