Canonical Allele Identifier: CA2172739488
Gene: ZNF106 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42451839A= , CM000677.2:g.42451839A= GRCh38
NC_000015.9:g.42744037A= , CM000677.1:g.42744037A= GRCh37
NC_000015.8:g.40531329A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000564754.7:c.433T= MANE Select ENSP00000456845.2:p.Trp145=
ENST00000263805.8:c.364T= ENSP00000263805.4:p.Trp122=
ENST00000564754.5:c.433T= ENSP00000456845.1:p.Trp145=
ENST00000565380.5:c.117-3134T= ENSP00000455674.1:n.117-3134T=
ENST00000565611.5:c.-13-3134T= ENSP00000457637.1:n.-13-3134T=
ENST00000565948.1:c.-288T= ENSP00000455049.1:n.-288T=
ENST00000567041.1:c.433T= ENSP00000454882.1:p.Trp145=
NM_001284306.1:c.-13-3134T= NP_001271235.1:n.-13-3134T=
NM_001284307.1:c.117-3134T= NP_001271236.1:n.117-3134T=
NM_022473.2:c.364T= NP_071918.1:p.Trp122=
XM_005254591.1:c.433T= XP_005254648.1:p.Trp145=
XM_005254592.1:c.433T= XP_005254649.1:p.Trp145=
NM_001284307.2:c.117-3134T= NP_001271236.1:n.117-3134T=
NM_001366844.1:c.117-3134T= NP_001353773.1:n.117-3134T=
NM_001366845.1:c.433T= NP_001353774.1:p.Trp145=
NM_001366846.1:c.433T= NP_001353775.1:p.Trp145=
XM_017022483.1:c.232T= XP_016877972.1:p.Trp78=
XM_017022484.2:c.-288T= XP_016877973.1:n.-288T=
NM_001284307.3:c.117-3134T= NP_001271236.1:n.117-3134T=
NM_001366844.2:c.117-3134T= NP_001353773.1:n.117-3134T=
NM_001366845.2:c.433T= NP_001353774.1:p.Trp145=
NM_001366846.2:c.433T= NP_001353775.1:p.Trp145=
NM_001284306.2:c.-13-3134T= NP_001271235.1:n.-13-3134T=
NM_001284307.4:c.117-3134T= NP_001271236.1:n.117-3134T=
NM_001366844.3:c.117-3134T= NP_001353773.1:n.117-3134T=
NM_001366845.3:c.433T= MANE Select NP_001353774.1:p.Trp145=
NM_001366846.3:c.433T= NP_001353775.1:p.Trp145=
NM_001381993.1:c.232T= NP_001368922.1:p.Trp78=
NM_001381994.1:c.318-3134T= NP_001368923.1:n.318-3134T=
NM_001381995.1:c.117-3134T= NP_001368924.1:n.117-3134T=
NM_001381996.1:c.60-3134T= NP_001368925.1:n.60-3134T=
NM_001381997.1:c.117-3134T= NP_001368926.1:n.117-3134T=
NM_001381998.1:c.117-3134T= NP_001368927.1:n.117-3134T=
NM_022473.3:c.364T= NP_071918.1:p.Trp122=