Canonical Allele Identifier: CA1016074406
Gene: KIZ HGNC NCBI

Linked Data

dbSNP Id: rs2032173407

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.21136160_21136161dup , CM000682.2:g.21136160_21136161dup GRCh38
NC_000020.10:g.21116801_21116802dup , CM000682.1:g.21116801_21116802dup GRCh37
NC_000020.9:g.21064801_21064802dup NCBI36
NG_033122.1:g.15178_15179dup
NG_033122.2:g.15181_15182dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000619189.5:c.153-230_153-229dup MANE Select ENSP00000479542.1:n.153-230_153-229dup
ENST00000611685.4:c.167-9405_167-9404dup
ENST00000612654.1:c.*61-230_*61-229dup ENSP00000480859.1:n.*61-230_*61-229dup
ENST00000616848.4:c.6+4001_6+4002dup ENSP00000480612.1:n.6+4001_6+4002dup
ENST00000619189.4:c.153-230_153-229dup ENSP00000479542.1:n.153-230_153-229dup
ENST00000619574.4:c.169-9405_169-9404dup ENSP00000484706.1:n.169-9405_169-9404dup
ENST00000620553.2:n.209-230_209-229dup
ENST00000620891.4:c.6+4001_6+4002dup ENSP00000478019.1:n.6+4001_6+4002dup
NM_001163022.1:c.6+4001_6+4002dup NP_001156494.1:n.6+4001_6+4002dup
NM_001163023.1:c.6+4001_6+4002dup NP_001156495.1:n.6+4001_6+4002dup
NM_001276389.1:c.169-9405_169-9404dup NP_001263318.1:n.169-9405_169-9404dup
NM_018474.4:c.153-230_153-229dup NP_060944.3:n.153-230_153-229dup
XM_011529296.1:c.153-230_153-229dup XP_011527598.1:n.153-230_153-229dup
XM_011529297.1:c.153-230_153-229dup XP_011527599.1:n.153-230_153-229dup
XM_011529298.1:c.153-230_153-229dup XP_011527600.1:n.153-230_153-229dup
XM_011529299.1:c.6+4001_6+4002dup XP_011527601.1:n.6+4001_6+4002dup
XR_937105.1:n.277-230_277-229dup
NM_001163022.2:c.6+4001_6+4002dup NP_001156494.1:n.6+4001_6+4002dup
NM_001163023.2:c.6+4001_6+4002dup NP_001156495.1:n.6+4001_6+4002dup
NM_001276389.2:c.169-9405_169-9404dup NP_001263318.1:n.169-9405_169-9404dup
NM_001352434.1:c.153-230_153-229dup NP_001339363.1:n.153-230_153-229dup
NM_001352435.1:c.6+4001_6+4002dup NP_001339364.1:n.6+4001_6+4002dup
NM_001352436.1:c.-234-230_-234-229dup NP_001339365.1:n.-234-230_-234-229dup
NM_018474.5:c.153-230_153-229dup NP_060944.3:n.153-230_153-229dup
XM_011529296.3:c.153-230_153-229dup XP_011527598.1:n.153-230_153-229dup
XM_011529297.3:c.153-230_153-229dup XP_011527599.1:n.153-230_153-229dup
XM_011529299.3:c.6+4001_6+4002dup XP_011527601.1:n.6+4001_6+4002dup
XM_017027951.2:c.-234-230_-234-229dup XP_016883440.1:n.-234-230_-234-229dup
XM_017027952.2:c.6+4001_6+4002dup XP_016883441.1:n.6+4001_6+4002dup
XR_001754334.2:n.219-230_219-229dup
XR_937105.3:n.219-230_219-229dup
NM_018474.6:c.153-230_153-229dup MANE Select NP_060944.3:n.153-230_153-229dup
NM_001163022.3:c.6+4001_6+4002dup NP_001156494.1:n.6+4001_6+4002dup
NM_001163023.3:c.6+4001_6+4002dup NP_001156495.1:n.6+4001_6+4002dup
NM_001352434.2:c.153-230_153-229dup NP_001339363.1:n.153-230_153-229dup
NM_001352435.2:c.6+4001_6+4002dup NP_001339364.1:n.6+4001_6+4002dup
NM_001352436.2:c.-234-230_-234-229dup NP_001339365.1:n.-234-230_-234-229dup