Canonical Allele Identifier: CA2078628643
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs1868828859

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23338097_23338099del , CM000675.2:g.23338097_23338099del GRCh38
NC_000013.10:g.23912236_23912238del , CM000675.1:g.23912236_23912238del GRCh37
NC_000013.9:g.22810236_22810238del NCBI36
NG_012342.1:g.100604_100606del

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+15686_2185+15688del ENSP00000508399.1:n.2185+15686_2185+15688...
ENST00000682944.1:c.5804_5806del ENSP00000507173.1:p.Ser1935_Val1936delins...
ENST00000683210.1:c.2185+15686_2185+15688del ENSP00000506739.1:n.2185+15686_2185+15688...
ENST00000683270.1:c.5768_5770del ENSP00000507624.1:p.Ser1923_Val1924delins...
ENST00000683367.1:c.2177-8615_2177-8613del ENSP00000507780.1:n.2177-8615_2177-8613de...
ENST00000683489.1:c.2291+3486_2291+3488del ENSP00000508403.1:n.2291+3486_2291+3488de...
ENST00000683680.1:c.2318+3486_2318+3488del ENSP00000507223.1:n.2318+3486_2318+3488de...
ENST00000684163.1:c.2204-8615_2204-8613del ENSP00000508262.1:n.2204-8615_2204-8613de...
ENST00000684196.1:n.4543-8615_4543-8613del
ENST00000684325.1:c.2185+15686_2185+15688del ENSP00000508121.1:n.2185+15686_2185+15688...
ENST00000684385.1:c.2221-8615_2221-8613del ENSP00000507855.1:n.2221-8615_2221-8613de...
ENST00000684497.1:c.2186-15455_2186-15453del ENSP00000507057.1:n.2186-15455_2186-15453...
ENST00000382292.9:c.5777_5779del MANE Select ENSP00000371729.3:p.Ser1926_Val1927delins...
ENST00000423156.2:c.2186-8615_2186-8613del ENSP00000390925.2:n.2186-8615_2186-8613de...
ENST00000455470.6:c.2431+3346_2431+3348del ENSP00000406565.2:n.2431+3346_2431+3348de...
ENST00000382292.7:c.5777_5779del ENSP00000371729.3:p.Ser1926_Val1927delins...
ENST00000382298.7:c.5777_5779del ENSP00000371735.3:p.Ser1926_Val1927delins...
ENST00000402364.1:c.3527_3529del ENSP00000385844.1:p.Ser1176_Val1177delins...
ENST00000423156.1:c.1058-8615_1058-8613del ENSP00000390925.1:n.1058-8615_1058-8613de...
ENST00000455470.5:c.2129+3346_2129+3348del
NM_001278055.1:c.5336_5338del NP_001264984.1:p.Ser1779_Val1780delinsIle...
NM_014363.5:c.5777_5779del NP_055178.3:p.Ser1926_Val1927delinsIle
XM_005266338.1:c.5804_5806del XP_005266395.1:p.Ser1935_Val1936delinsIle...
XM_011535038.1:c.5828_5830del XP_011533340.1:p.Ser1943_Val1944delinsIle...
XM_011535039.1:c.5795_5797del XP_011533341.1:p.Ser1932_Val1933delinsIle...
XM_005266338.2:c.5804_5806del XP_005266395.1:p.Ser1935_Val1936delinsIle...
XM_011535039.2:c.5795_5797del XP_011533341.1:p.Ser1932_Val1933delinsIle...
XM_017020539.1:c.5768_5770del XP_016876028.1:p.Ser1923_Val1924delinsIle...
XM_024449337.1:c.5804_5806del XP_024305105.1:p.Ser1935_Val1936delinsIle...
NM_014363.6:c.5777_5779del MANE Select NP_055178.3:p.Ser1926_Val1927delinsIle
NM_001278055.2:c.5336_5338del NP_001264984.1:p.Ser1779_Val1780delinsIle...