Canonical Allele Identifier: CA2078625134
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23336289G= , CM000675.2:g.23336289G= GRCh38
NC_000013.10:g.23910428G= , CM000675.1:g.23910428G= GRCh37
NC_000013.9:g.22808428G= NCBI36
NG_012342.1:g.102414C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+17496C= ENSP00000508399.1:n.2185+17496C=
ENST00000682944.1:c.7614C= ENSP00000507173.1:p.Thr2538=
ENST00000683210.1:c.2185+17496C= ENSP00000506739.1:n.2185+17496C=
ENST00000683270.1:c.6445+1133C= ENSP00000507624.1:n.6445+1133C=
ENST00000683367.1:c.2177-6805C= ENSP00000507780.1:n.2177-6805C=
ENST00000683489.1:c.2291+5296C= ENSP00000508403.1:n.2291+5296C=
ENST00000683680.1:c.2318+5296C= ENSP00000507223.1:n.2318+5296C=
ENST00000684163.1:c.2204-6805C= ENSP00000508262.1:n.2204-6805C=
ENST00000684196.1:n.4543-6805C=
ENST00000684325.1:c.2186-14615C= ENSP00000508121.1:n.2186-14615C=
ENST00000684385.1:c.2221-6805C= ENSP00000507855.1:n.2221-6805C=
ENST00000684497.1:c.2186-13645C= ENSP00000507057.1:n.2186-13645C=
ENST00000382292.9:c.7587C= MANE Select ENSP00000371729.3:p.Thr2529=
ENST00000423156.2:c.2186-6805C= ENSP00000390925.2:n.2186-6805C=
ENST00000455470.6:c.2431+5156C= ENSP00000406565.2:n.2431+5156C=
ENST00000382292.7:c.7587C= ENSP00000371729.3:p.Thr2529=
ENST00000382298.7:c.7587C= ENSP00000371735.3:p.Thr2529=
ENST00000402364.1:c.5337C= ENSP00000385844.1:p.Thr1779=
ENST00000423156.1:c.1058-6805C= ENSP00000390925.1:n.1058-6805C=
ENST00000455470.5:c.2129+5156C=
NM_001278055.1:c.7146C= NP_001264984.1:p.Thr2382=
NM_014363.5:c.7587C= NP_055178.3:p.Thr2529=
XM_005266338.1:c.7614C= XP_005266395.1:p.Thr2538=
XM_011535038.1:c.7638C= XP_011533340.1:p.Thr2546=
XM_011535039.1:c.7605C= XP_011533341.1:p.Thr2535=
XM_005266338.2:c.7614C= XP_005266395.1:p.Thr2538=
XM_011535039.2:c.7605C= XP_011533341.1:p.Thr2535=
XM_017020539.1:c.7578C= XP_016876028.1:p.Thr2526=
XM_024449337.1:c.7614C= XP_024305105.1:p.Thr2538=
NM_014363.6:c.7587C= MANE Select NP_055178.3:p.Thr2529=
NM_001278055.2:c.7146C= NP_001264984.1:p.Thr2382=