Canonical Allele Identifier: CA2078641235
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23339842T= , CM000675.2:g.23339842T= GRCh38
NC_000013.10:g.23913981T= , CM000675.1:g.23913981T= GRCh37
NC_000013.9:g.22811981T= NCBI36
NG_012342.1:g.98861A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+13943A= ENSP00000508399.1:n.2185+13943A=
ENST00000682944.1:c.4061A= ENSP00000507173.1:p.Gln1354=
ENST00000683210.1:c.2185+13943A= ENSP00000506739.1:n.2185+13943A=
ENST00000683270.1:c.4025A= ENSP00000507624.1:p.Gln1342=
ENST00000683367.1:c.2177-10358A= ENSP00000507780.1:n.2177-10358A=
ENST00000683489.1:c.2291+1743A= ENSP00000508403.1:n.2291+1743A=
ENST00000683680.1:c.2318+1743A= ENSP00000507223.1:n.2318+1743A=
ENST00000684163.1:c.2203+6969A= ENSP00000508262.1:n.2203+6969A=
ENST00000684196.1:n.4543-10358A=
ENST00000684325.1:c.2185+13943A= ENSP00000508121.1:n.2185+13943A=
ENST00000684385.1:c.2220+6969A= ENSP00000507855.1:n.2220+6969A=
ENST00000684497.1:c.2185+13943A= ENSP00000507057.1:n.2185+13943A=
ENST00000382292.9:c.4034A= MANE Select ENSP00000371729.3:p.Gln1345=
ENST00000423156.2:c.2186-10358A= ENSP00000390925.2:n.2186-10358A=
ENST00000455470.6:c.2431+1603A= ENSP00000406565.2:n.2431+1603A=
ENST00000382292.7:c.4034A= ENSP00000371729.3:p.Gln1345=
ENST00000382298.7:c.4034A= ENSP00000371735.3:p.Gln1345=
ENST00000402364.1:c.1784A= ENSP00000385844.1:p.Gln595=
ENST00000423156.1:c.1058-10358A= ENSP00000390925.1:n.1058-10358A=
ENST00000455470.5:c.2129+1603A=
NM_001278055.1:c.3593A= NP_001264984.1:p.Gln1198=
NM_014363.5:c.4034A= NP_055178.3:p.Gln1345=
XM_005266338.1:c.4061A= XP_005266395.1:p.Gln1354=
XM_011535038.1:c.4085A= XP_011533340.1:p.Gln1362=
XM_011535039.1:c.4052A= XP_011533341.1:p.Gln1351=
XM_005266338.2:c.4061A= XP_005266395.1:p.Gln1354=
XM_011535039.2:c.4052A= XP_011533341.1:p.Gln1351=
XM_017020539.1:c.4025A= XP_016876028.1:p.Gln1342=
XM_024449337.1:c.4061A= XP_024305105.1:p.Gln1354=
NM_014363.6:c.4034A= MANE Select NP_055178.3:p.Gln1345=
NM_001278055.2:c.3593A= NP_001264984.1:p.Gln1198=