Canonical Allele Identifier: CA408488544
Gene: KIZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.21136488T>G , CM000682.2:g.21136488T>G GRCh38
NC_000020.10:g.21117129T>G , CM000682.1:g.21117129T>G GRCh37
NC_000020.9:g.21065129T>G NCBI36
NG_033122.1:g.15506T>G
NG_033122.2:g.15509T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000619189.5:c.251T>G MANE Select ENSP00000479542.1:p.Phe84Cys
ENST00000611685.4:c.167-9077T>G
ENST00000616848.4:c.6+4329T>G ENSP00000480612.1:n.6+4329T>G
ENST00000619189.4:c.251T>G ENSP00000479542.1:p.Phe84Cys
ENST00000619574.4:c.169-9077T>G ENSP00000484706.1:n.169-9077T>G
ENST00000620553.2:n.307T>G
ENST00000620891.4:c.6+4329T>G ENSP00000478019.1:n.6+4329T>G
NM_001163022.1:c.6+4329T>G NP_001156494.1:n.6+4329T>G
NM_001163023.1:c.6+4329T>G NP_001156495.1:n.6+4329T>G
NM_001276389.1:c.169-9077T>G NP_001263318.1:n.169-9077T>G
NM_018474.4:c.251T>G NP_060944.3:p.Phe84Cys
XM_011529296.1:c.251T>G XP_011527598.1:p.Phe84Cys
XM_011529297.1:c.251T>G XP_011527599.1:p.Phe84Cys
XM_011529298.1:c.251T>G XP_011527600.1:p.Phe84Cys
XM_011529299.1:c.6+4329T>G XP_011527601.1:n.6+4329T>G
XR_937105.1:n.375T>G
NM_001163022.2:c.6+4329T>G NP_001156494.1:n.6+4329T>G
NM_001163023.2:c.6+4329T>G NP_001156495.1:n.6+4329T>G
NM_001276389.2:c.169-9077T>G NP_001263318.1:n.169-9077T>G
NM_001352434.1:c.251T>G NP_001339363.1:p.Phe84Cys
NM_001352435.1:c.6+4329T>G NP_001339364.1:n.6+4329T>G
NM_001352436.1:c.-136T>G NP_001339365.1:n.-136T>G
NM_018474.5:c.251T>G NP_060944.3:p.Phe84Cys
XM_011529296.3:c.251T>G XP_011527598.1:p.Phe84Cys
XM_011529297.3:c.251T>G XP_011527599.1:p.Phe84Cys
XM_011529299.3:c.6+4329T>G XP_011527601.1:n.6+4329T>G
XM_017027951.2:c.-136T>G XP_016883440.1:n.-136T>G
XM_017027952.2:c.6+4329T>G XP_016883441.1:n.6+4329T>G
XR_001754334.2:n.317T>G
XR_937105.3:n.317T>G
NM_018474.6:c.251T>G MANE Select NP_060944.3:p.Phe84Cys
NM_001163022.3:c.6+4329T>G NP_001156494.1:n.6+4329T>G
NM_001163023.3:c.6+4329T>G NP_001156495.1:n.6+4329T>G
NM_001352434.2:c.251T>G NP_001339363.1:p.Phe84Cys
NM_001352435.2:c.6+4329T>G NP_001339364.1:n.6+4329T>G
NM_001352436.2:c.-136T>G NP_001339365.1:n.-136T>G