Canonical Allele Identifier: CA9726797
Gene: SNPH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1300587A>T , CM000682.2:g.1300587A>T GRCh38
NC_000020.10:g.1281231A>T , CM000682.1:g.1281231A>T GRCh37
NC_000020.9:g.1229231A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381867.6:c.316A>T MANE Select ENSP00000371291.1:p.Ser106Cys
ENST00000649598.1:c.283A>T ENSP00000496966.1:p.Ser95Cys
ENST00000381867.5:c.316A>T ENSP00000371291.1:p.Ser106Cys
ENST00000381873.7:c.184A>T ENSP00000371297.3:p.Ser62Cys
ENST00000614659.1:c.316A>T ENSP00000479696.1:p.Ser106Cys
NM_014723.2:c.184A>T NP_055538.2:p.Ser62Cys
XM_005260888.2:c.316A>T XP_005260945.1:p.Ser106Cys
XM_005260889.2:c.283A>T XP_005260946.1:p.Ser95Cys
XM_011529402.1:c.415A>T XP_011527704.1:p.Ser139Cys
XM_011529403.1:c.415A>T XP_011527705.1:p.Ser139Cys
XM_011529404.1:c.283A>T XP_011527706.1:p.Ser95Cys
XM_011529405.1:c.283A>T XP_011527707.1:p.Ser95Cys
XM_011529406.1:c.283A>T XP_011527708.1:p.Ser95Cys
NM_001318234.1:c.316A>T NP_001305163.1:p.Ser106Cys
NM_014723.3:c.184A>T NP_055538.2:p.Ser62Cys
XM_005260889.3:c.283A>T XP_005260946.1:p.Ser95Cys
XM_011529402.2:c.415A>T XP_011527704.1:p.Ser139Cys
XM_011529403.2:c.415A>T XP_011527705.1:p.Ser139Cys
XM_011529404.2:c.283A>T XP_011527706.1:p.Ser95Cys
NM_001318234.2:c.316A>T MANE Select NP_001305163.1:p.Ser106Cys
NM_014723.4:c.184A>T NP_055538.2:p.Ser62Cys