Canonical Allele Identifier: CA6911502
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2062913
ClinVar RCV Id: RCV002958105
dbSNP Id: rs761453388

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23340299T>C , CM000675.2:g.23340299T>C GRCh38
NC_000013.10:g.23914438T>C , CM000675.1:g.23914438T>C GRCh37
NC_000013.9:g.22812438T>C NCBI36
NG_012342.1:g.98404A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+13486A>G ENSP00000508399.1:n.2185+13486A>G
ENST00000682944.1:c.3604A>G ENSP00000507173.1:p.Ile1202Val
ENST00000683210.1:c.2185+13486A>G ENSP00000506739.1:n.2185+13486A>G
ENST00000683270.1:c.3568A>G ENSP00000507624.1:p.Ile1190Val
ENST00000683367.1:c.2177-10815A>G ENSP00000507780.1:n.2177-10815A>G
ENST00000683489.1:c.2291+1286A>G ENSP00000508403.1:n.2291+1286A>G
ENST00000683680.1:c.2318+1286A>G ENSP00000507223.1:n.2318+1286A>G
ENST00000684163.1:c.2203+6512A>G ENSP00000508262.1:n.2203+6512A>G
ENST00000684196.1:n.4543-10815A>G
ENST00000684325.1:c.2185+13486A>G ENSP00000508121.1:n.2185+13486A>G
ENST00000684385.1:c.2220+6512A>G ENSP00000507855.1:n.2220+6512A>G
ENST00000684497.1:c.2185+13486A>G ENSP00000507057.1:n.2185+13486A>G
ENST00000382292.9:c.3577A>G MANE Select ENSP00000371729.3:p.Ile1193Val
ENST00000423156.2:c.2186-10815A>G ENSP00000390925.2:n.2186-10815A>G
ENST00000455470.6:c.2431+1146A>G ENSP00000406565.2:n.2431+1146A>G
ENST00000382292.7:c.3577A>G ENSP00000371729.3:p.Ile1193Val
ENST00000382298.7:c.3577A>G ENSP00000371735.3:p.Ile1193Val
ENST00000402364.1:c.1327A>G ENSP00000385844.1:p.Ile443Val
ENST00000423156.1:c.1058-10815A>G ENSP00000390925.1:n.1058-10815A>G
ENST00000455470.5:c.2129+1146A>G
NM_001278055.1:c.3136A>G NP_001264984.1:p.Ile1046Val
NM_014363.5:c.3577A>G NP_055178.3:p.Ile1193Val
XM_005266338.1:c.3604A>G XP_005266395.1:p.Ile1202Val
XM_011535038.1:c.3628A>G XP_011533340.1:p.Ile1210Val
XM_011535039.1:c.3595A>G XP_011533341.1:p.Ile1199Val
XM_005266338.2:c.3604A>G XP_005266395.1:p.Ile1202Val
XM_011535039.2:c.3595A>G XP_011533341.1:p.Ile1199Val
XM_017020539.1:c.3568A>G XP_016876028.1:p.Ile1190Val
XM_024449337.1:c.3604A>G XP_024305105.1:p.Ile1202Val
NM_014363.6:c.3577A>G MANE Select NP_055178.3:p.Ile1193Val
NM_001278055.2:c.3136A>G NP_001264984.1:p.Ile1046Val