Canonical Allele Identifier: CA407986154

Gene: SNPH

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1305612G>A , CM000682.2:g.1305612G>A	GRCh38
NC_000020.10:g.1286256G>A , CM000682.1:g.1286256G>A	GRCh37
NC_000020.9:g.1234256G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381867.6:c.1175G>A MANE Select	ENSP00000371291.1:p.Cys392Tyr
ENST00000649598.1:c.1142G>A	ENSP00000496966.1:p.Cys381Tyr
ENST00000381867.5:c.1175G>A	ENSP00000371291.1:p.Cys392Tyr
ENST00000381873.7:c.1043G>A	ENSP00000371297.3:p.Cys348Tyr
ENST00000614659.1:c.1175G>A	ENSP00000479696.1:p.Cys392Tyr
NM_014723.2:c.1043G>A	NP_055538.2:p.Cys348Tyr
XM_005260888.2:c.1175G>A	XP_005260945.1:p.Cys392Tyr
XM_005260889.2:c.1142G>A	XP_005260946.1:p.Cys381Tyr
XM_011529402.1:c.1274G>A	XP_011527704.1:p.Cys425Tyr
XM_011529403.1:c.1274G>A	XP_011527705.1:p.Cys425Tyr
XM_011529404.1:c.1142G>A	XP_011527706.1:p.Cys381Tyr
XM_011529405.1:c.1142G>A	XP_011527707.1:p.Cys381Tyr
XM_011529406.1:c.1142G>A	XP_011527708.1:p.Cys381Tyr
NM_001318234.1:c.1175G>A	NP_001305163.1:p.Cys392Tyr
NM_014723.3:c.1043G>A	NP_055538.2:p.Cys348Tyr
XM_005260889.3:c.1142G>A	XP_005260946.1:p.Cys381Tyr
XM_011529402.2:c.1274G>A	XP_011527704.1:p.Cys425Tyr
XM_011529403.2:c.1274G>A	XP_011527705.1:p.Cys425Tyr
XM_011529404.2:c.1142G>A	XP_011527706.1:p.Cys381Tyr
NM_001318234.2:c.1175G>A MANE Select	NP_001305163.1:p.Cys392Tyr
NM_014723.4:c.1043G>A	NP_055538.2:p.Cys348Tyr