Canonical Allele Identifier: CA310751172
Gene: SNPH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1305047G>A , CM000682.2:g.1305047G>A GRCh38
NC_000020.10:g.1285691G>A , CM000682.1:g.1285691G>A GRCh37
NC_000020.9:g.1233691G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381867.6:c.610G>A MANE Select ENSP00000371291.1:p.Asp204Asn
ENST00000649598.1:c.577G>A ENSP00000496966.1:p.Asp193Asn
ENST00000381867.5:c.610G>A ENSP00000371291.1:p.Asp204Asn
ENST00000381873.7:c.478G>A ENSP00000371297.3:p.Asp160Asn
ENST00000614659.1:c.610G>A ENSP00000479696.1:p.Asp204Asn
NM_014723.2:c.478G>A NP_055538.2:p.Asp160Asn
XM_005260888.2:c.610G>A XP_005260945.1:p.Asp204Asn
XM_005260889.2:c.577G>A XP_005260946.1:p.Asp193Asn
XM_011529402.1:c.709G>A XP_011527704.1:p.Asp237Asn
XM_011529403.1:c.709G>A XP_011527705.1:p.Asp237Asn
XM_011529404.1:c.577G>A XP_011527706.1:p.Asp193Asn
XM_011529405.1:c.577G>A XP_011527707.1:p.Asp193Asn
XM_011529406.1:c.577G>A XP_011527708.1:p.Asp193Asn
NM_001318234.1:c.610G>A NP_001305163.1:p.Asp204Asn
NM_014723.3:c.478G>A NP_055538.2:p.Asp160Asn
XM_005260889.3:c.577G>A XP_005260946.1:p.Asp193Asn
XM_011529402.2:c.709G>A XP_011527704.1:p.Asp237Asn
XM_011529403.2:c.709G>A XP_011527705.1:p.Asp237Asn
XM_011529404.2:c.577G>A XP_011527706.1:p.Asp193Asn
NM_001318234.2:c.610G>A MANE Select NP_001305163.1:p.Asp204Asn
NM_014723.4:c.478G>A NP_055538.2:p.Asp160Asn