Canonical Allele Identifier: CA6911906
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448194
dbSNP Id: rs372022664

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23355093T>C , CM000675.2:g.23355093T>C GRCh38
NC_000013.10:g.23929232T>C , CM000675.1:g.23929232T>C GRCh37
NC_000013.9:g.22827232T>C NCBI36
NG_012342.1:g.83610A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.1519A>G ENSP00000508399.1:p.Thr507Ala
ENST00000682944.1:c.1519A>G ENSP00000507173.1:p.Thr507Ala
ENST00000683154.1:n.1657A>G
ENST00000683210.1:c.1519A>G ENSP00000506739.1:p.Thr507Ala
ENST00000683270.1:c.1510A>G ENSP00000507624.1:p.Thr504Ala
ENST00000683367.1:c.1510A>G ENSP00000507780.1:p.Thr504Ala
ENST00000683489.1:c.1519A>G ENSP00000508403.1:p.Thr507Ala
ENST00000683680.1:c.1519A>G ENSP00000507223.1:p.Thr507Ala
ENST00000684163.1:c.1510A>G ENSP00000508262.1:p.Thr504Ala
ENST00000684196.1:n.3876A>G
ENST00000684325.1:c.1519A>G ENSP00000508121.1:p.Thr507Ala
ENST00000684385.1:c.1519A>G ENSP00000507855.1:p.Thr507Ala
ENST00000684497.1:c.1519A>G ENSP00000507057.1:p.Thr507Ala
ENST00000382292.9:c.1519A>G MANE Select ENSP00000371729.3:p.Thr507Ala
ENST00000423156.2:c.1519A>G ENSP00000390925.2:p.Thr507Ala
ENST00000455470.6:c.1519A>G ENSP00000406565.2:p.Thr507Ala
ENST00000382292.7:c.1519A>G ENSP00000371729.3:p.Thr507Ala
ENST00000382298.7:c.1519A>G ENSP00000371735.3:p.Thr507Ala
ENST00000402364.1:c.-732A>G ENSP00000385844.1:n.-732A>G
ENST00000423156.1:c.391A>G ENSP00000390925.1:p.Thr131Ala
ENST00000455470.5:c.1217A>G
NM_001278055.1:c.1078A>G NP_001264984.1:p.Thr360Ala
NM_014363.5:c.1519A>G NP_055178.3:p.Thr507Ala
XM_005266338.1:c.1519A>G XP_005266395.1:p.Thr507Ala
XM_011535038.1:c.1543A>G XP_011533340.1:p.Thr515Ala
XM_011535039.1:c.1510A>G XP_011533341.1:p.Thr504Ala
XM_005266338.2:c.1519A>G XP_005266395.1:p.Thr507Ala
XM_011535039.2:c.1510A>G XP_011533341.1:p.Thr504Ala
XM_017020539.1:c.1510A>G XP_016876028.1:p.Thr504Ala
XM_024449337.1:c.1519A>G XP_024305105.1:p.Thr507Ala
NM_014363.6:c.1519A>G MANE Select NP_055178.3:p.Thr507Ala
NM_001278055.2:c.1078A>G NP_001264984.1:p.Thr360Ala