Canonical Allele Identifier: CA2078626379
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23336841G= , CM000675.2:g.23336841G= GRCh38
NC_000013.10:g.23910980G= , CM000675.1:g.23910980G= GRCh37
NC_000013.9:g.22808980G= NCBI36
NG_012342.1:g.101862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+16944C= ENSP00000508399.1:n.2185+16944C=
ENST00000682944.1:c.7062C= ENSP00000507173.1:p.Ser2354=
ENST00000683210.1:c.2185+16944C= ENSP00000506739.1:n.2185+16944C=
ENST00000683270.1:c.6445+581C= ENSP00000507624.1:n.6445+581C=
ENST00000683367.1:c.2177-7357C= ENSP00000507780.1:n.2177-7357C=
ENST00000683489.1:c.2291+4744C= ENSP00000508403.1:n.2291+4744C=
ENST00000683680.1:c.2318+4744C= ENSP00000507223.1:n.2318+4744C=
ENST00000684163.1:c.2204-7357C= ENSP00000508262.1:n.2204-7357C=
ENST00000684196.1:n.4543-7357C=
ENST00000684325.1:c.2186-15167C= ENSP00000508121.1:n.2186-15167C=
ENST00000684385.1:c.2221-7357C= ENSP00000507855.1:n.2221-7357C=
ENST00000684497.1:c.2186-14197C= ENSP00000507057.1:n.2186-14197C=
ENST00000382292.9:c.7035C= MANE Select ENSP00000371729.3:p.Ser2345=
ENST00000423156.2:c.2186-7357C= ENSP00000390925.2:n.2186-7357C=
ENST00000455470.6:c.2431+4604C= ENSP00000406565.2:n.2431+4604C=
ENST00000382292.7:c.7035C= ENSP00000371729.3:p.Ser2345=
ENST00000382298.7:c.7035C= ENSP00000371735.3:p.Ser2345=
ENST00000402364.1:c.4785C= ENSP00000385844.1:p.Ser1595=
ENST00000423156.1:c.1058-7357C= ENSP00000390925.1:n.1058-7357C=
ENST00000455470.5:c.2129+4604C=
NM_001278055.1:c.6594C= NP_001264984.1:p.Ser2198=
NM_014363.5:c.7035C= NP_055178.3:p.Ser2345=
XM_005266338.1:c.7062C= XP_005266395.1:p.Ser2354=
XM_011535038.1:c.7086C= XP_011533340.1:p.Ser2362=
XM_011535039.1:c.7053C= XP_011533341.1:p.Ser2351=
XM_005266338.2:c.7062C= XP_005266395.1:p.Ser2354=
XM_011535039.2:c.7053C= XP_011533341.1:p.Ser2351=
XM_017020539.1:c.7026C= XP_016876028.1:p.Ser2342=
XM_024449337.1:c.7062C= XP_024305105.1:p.Ser2354=
NM_014363.6:c.7035C= MANE Select NP_055178.3:p.Ser2345=
NM_001278055.2:c.6594C= NP_001264984.1:p.Ser2198=