Canonical Allele Identifier: CA387532907
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23339848C>G , CM000675.2:g.23339848C>G GRCh38
NC_000013.10:g.23913987C>G , CM000675.1:g.23913987C>G GRCh37
NC_000013.9:g.22811987C>G NCBI36
NG_012342.1:g.98855G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+13937G>C ENSP00000508399.1:n.2185+13937G>C
ENST00000682944.1:c.4055G>C ENSP00000507173.1:p.Ser1352Thr
ENST00000683210.1:c.2185+13937G>C ENSP00000506739.1:n.2185+13937G>C
ENST00000683270.1:c.4019G>C ENSP00000507624.1:p.Ser1340Thr
ENST00000683367.1:c.2177-10364G>C ENSP00000507780.1:n.2177-10364G>C
ENST00000683489.1:c.2291+1737G>C ENSP00000508403.1:n.2291+1737G>C
ENST00000683680.1:c.2318+1737G>C ENSP00000507223.1:n.2318+1737G>C
ENST00000684163.1:c.2203+6963G>C ENSP00000508262.1:n.2203+6963G>C
ENST00000684196.1:n.4543-10364G>C
ENST00000684325.1:c.2185+13937G>C ENSP00000508121.1:n.2185+13937G>C
ENST00000684385.1:c.2220+6963G>C ENSP00000507855.1:n.2220+6963G>C
ENST00000684497.1:c.2185+13937G>C ENSP00000507057.1:n.2185+13937G>C
ENST00000382292.9:c.4028G>C MANE Select ENSP00000371729.3:p.Ser1343Thr
ENST00000423156.2:c.2186-10364G>C ENSP00000390925.2:n.2186-10364G>C
ENST00000455470.6:c.2431+1597G>C ENSP00000406565.2:n.2431+1597G>C
ENST00000382292.7:c.4028G>C ENSP00000371729.3:p.Ser1343Thr
ENST00000382298.7:c.4028G>C ENSP00000371735.3:p.Ser1343Thr
ENST00000402364.1:c.1778G>C ENSP00000385844.1:p.Ser593Thr
ENST00000423156.1:c.1058-10364G>C ENSP00000390925.1:n.1058-10364G>C
ENST00000455470.5:c.2129+1597G>C
NM_001278055.1:c.3587G>C NP_001264984.1:p.Ser1196Thr
NM_014363.5:c.4028G>C NP_055178.3:p.Ser1343Thr
XM_005266338.1:c.4055G>C XP_005266395.1:p.Ser1352Thr
XM_011535038.1:c.4079G>C XP_011533340.1:p.Ser1360Thr
XM_011535039.1:c.4046G>C XP_011533341.1:p.Ser1349Thr
XM_005266338.2:c.4055G>C XP_005266395.1:p.Ser1352Thr
XM_011535039.2:c.4046G>C XP_011533341.1:p.Ser1349Thr
XM_017020539.1:c.4019G>C XP_016876028.1:p.Ser1340Thr
XM_024449337.1:c.4055G>C XP_024305105.1:p.Ser1352Thr
NM_014363.6:c.4028G>C MANE Select NP_055178.3:p.Ser1343Thr
NM_001278055.2:c.3587G>C NP_001264984.1:p.Ser1196Thr