Canonical Allele Identifier: CA2078641956
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23340226G= , CM000675.2:g.23340226G= GRCh38
NC_000013.10:g.23914365G= , CM000675.1:g.23914365G= GRCh37
NC_000013.9:g.22812365G= NCBI36
NG_012342.1:g.98477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+13559C= ENSP00000508399.1:n.2185+13559C=
ENST00000682944.1:c.3677C= ENSP00000507173.1:p.Thr1226=
ENST00000683210.1:c.2185+13559C= ENSP00000506739.1:n.2185+13559C=
ENST00000683270.1:c.3641C= ENSP00000507624.1:p.Thr1214=
ENST00000683367.1:c.2177-10742C= ENSP00000507780.1:n.2177-10742C=
ENST00000683489.1:c.2291+1359C= ENSP00000508403.1:n.2291+1359C=
ENST00000683680.1:c.2318+1359C= ENSP00000507223.1:n.2318+1359C=
ENST00000684163.1:c.2203+6585C= ENSP00000508262.1:n.2203+6585C=
ENST00000684196.1:n.4543-10742C=
ENST00000684325.1:c.2185+13559C= ENSP00000508121.1:n.2185+13559C=
ENST00000684385.1:c.2220+6585C= ENSP00000507855.1:n.2220+6585C=
ENST00000684497.1:c.2185+13559C= ENSP00000507057.1:n.2185+13559C=
ENST00000382292.9:c.3650C= MANE Select ENSP00000371729.3:p.Thr1217=
ENST00000423156.2:c.2186-10742C= ENSP00000390925.2:n.2186-10742C=
ENST00000455470.6:c.2431+1219C= ENSP00000406565.2:n.2431+1219C=
ENST00000382292.7:c.3650C= ENSP00000371729.3:p.Thr1217=
ENST00000382298.7:c.3650C= ENSP00000371735.3:p.Thr1217=
ENST00000402364.1:c.1400C= ENSP00000385844.1:p.Thr467=
ENST00000423156.1:c.1058-10742C= ENSP00000390925.1:n.1058-10742C=
ENST00000455470.5:c.2129+1219C=
NM_001278055.1:c.3209C= NP_001264984.1:p.Thr1070=
NM_014363.5:c.3650C= NP_055178.3:p.Thr1217=
XM_005266338.1:c.3677C= XP_005266395.1:p.Thr1226=
XM_011535038.1:c.3701C= XP_011533340.1:p.Thr1234=
XM_011535039.1:c.3668C= XP_011533341.1:p.Thr1223=
XM_005266338.2:c.3677C= XP_005266395.1:p.Thr1226=
XM_011535039.2:c.3668C= XP_011533341.1:p.Thr1223=
XM_017020539.1:c.3641C= XP_016876028.1:p.Thr1214=
XM_024449337.1:c.3677C= XP_024305105.1:p.Thr1226=
NM_014363.6:c.3650C= MANE Select NP_055178.3:p.Thr1217=
NM_001278055.2:c.3209C= NP_001264984.1:p.Thr1070=