Canonical Allele Identifier: CA2008178
Community Standard Title: NM_152520.6(ZNF385B):c.539G>A (p.Arg180His)
Gene: ZNF385B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.179518541C>T , CM000664.2:g.179518541C>T GRCh38
NC_000002.11:g.180383268C>T , CM000664.1:g.180383268C>T GRCh37
NC_000002.10:g.180091513C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_152520.6:c.539G>A MANE Select NP_689733.4:p.Arg180His
ENST00000410066.7:c.539G>A MANE Select ENSP00000386845.2:p.Arg180His
NM_001113397.1:c.266G>A NP_001106868.1:p.Arg89His
NM_001113397.2:c.266G>A NP_001106868.1:p.Arg89His
NM_001113398.1:c.188G>A NP_001106869.1:p.Arg63His
NM_001113398.2:c.188G>A NP_001106869.1:p.Arg63His
NM_001113398.3:c.188G>A NP_001106869.1:p.Arg63His
NM_001282725.1:c.188G>A NP_001269654.1:p.Arg63His
NM_001282725.2:c.188G>A NP_001269654.1:p.Arg63His
NM_001282725.3:c.188G>A NP_001269654.1:p.Arg63His
NM_001352808.1:c.539G>A NP_001339737.1:p.Arg180His
NM_001352808.2:c.539G>A NP_001339737.1:p.Arg180His
NM_001352809.1:c.677G>A NP_001339738.1:p.Arg226His
NM_001352809.2:c.677G>A NP_001339738.1:p.Arg226His
NM_001352810.1:c.539G>A NP_001339739.1:p.Arg180His
NM_001352810.2:c.539G>A NP_001339739.1:p.Arg180His
NM_001352811.1:c.578G>A NP_001339740.1:p.Arg193His
NM_001352811.2:c.578G>A NP_001339740.1:p.Arg193His
NM_001352812.1:c.290G>A NP_001339741.1:p.Arg97His
NM_001352812.2:c.290G>A NP_001339741.1:p.Arg97His
NM_001352813.1:c.188G>A NP_001339742.1:p.Arg63His
NM_001352813.2:c.188G>A NP_001339742.1:p.Arg63His
NM_001352814.1:c.188G>A NP_001339743.1:p.Arg63His
NM_001352814.2:c.188G>A NP_001339743.1:p.Arg63His
NM_001352815.1:c.188G>A NP_001339744.1:p.Arg63His
NM_001352816.1:c.152G>A NP_001339745.1:p.Arg51His
NM_001352816.2:c.152G>A NP_001339745.1:p.Arg51His
NM_001352817.1:c.98G>A NP_001339746.1:p.Arg33His
NM_152520.4:c.494G>A NP_689733.3:p.Arg165His
NM_152520.5:c.539G>A NP_689733.4:p.Arg180His
NR_104234.1:n.607G>A
NR_104234.2:n.607G>A
NR_148054.1:n.1098G>A
NR_148054.2:n.1205G>A
NR_148055.1:n.434G>A
NR_148055.2:n.431G>A
NR_148056.1:n.1098G>A
NR_148056.2:n.1205G>A
NR_148057.1:n.955G>A
NR_148057.2:n.1062G>A
NR_148058.1:n.1137G>A
NR_148058.2:n.1244G>A
NR_148059.1:n.896G>A
ENST00000336917.9:c.188G>A ENSP00000338225.5:p.Arg63His
ENST00000409343.5:c.266G>A ENSP00000386379.1:p.Arg89His
ENST00000409692.5:c.188G>A ENSP00000386507.1:p.Arg63His
ENST00000410066.5:c.494G>A ENSP00000386845.1:p.Arg165His
ENST00000439340.1:c.287G>A ENSP00000399198.1:p.Arg96His
ENST00000457304.5:c.188G>A ENSP00000394038.1:p.Arg63His
ENST00000466398.5:n.606G>A
ENST00000469551.5:n.463G>A
ENST00000475539.5:n.240G>A
ENST00000495289.1:n.266G>A
XM_011510713.1:c.578G>A XP_011509015.1:p.Arg193His
XM_011510713.3:c.578G>A XP_011509015.1:p.Arg193His
XM_011510714.1:c.539G>A XP_011509016.1:p.Arg180His
XM_011510715.1:c.578G>A XP_011509017.1:p.Arg193His
XM_011510716.1:c.287G>A XP_011509018.1:p.Arg96His
XM_011510716.2:c.287G>A XP_011509018.1:p.Arg96His
XM_011510717.1:c.287G>A XP_011509019.1:p.Arg96His
XM_011510717.2:c.287G>A XP_011509019.1:p.Arg96His
XM_011510718.1:c.227G>A XP_011509020.1:p.Arg76His
XM_011510719.1:c.227G>A XP_011509021.1:p.Arg76His
XM_011510719.2:c.227G>A XP_011509021.1:p.Arg76His
XM_011510720.1:c.227G>A XP_011509022.1:p.Arg76His
XM_011510720.2:c.227G>A XP_011509022.1:p.Arg76His
XM_011510721.1:c.188G>A XP_011509023.1:p.Arg63His
XM_011510721.3:c.188G>A XP_011509023.1:p.Arg63His
XM_011510723.1:c.578G>A XP_011509025.1:p.Arg193His
XM_011510723.2:c.578G>A XP_011509025.1:p.Arg193His
XM_017003441.2:c.539G>A XP_016858930.1:p.Arg180His