Canonical Allele Identifier: CA954036686
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23331572_23331573insCAATTTGATTTCTGACACTTCATATCAAATTGTCAGTTGCTGATTTAAGAGTCATTGCCAG , CM000675.2:g.23331572_23331573insCAATTTGATTTCTGACACTTCATATCAAATTGTCAGTTGCTGATTTAAGAGTCATTGCCAG GRCh38
NC_000013.10:g.23905711_23905712insCAATTTGATTTCTGACACTTCATATCAAATTGTCAGTTGCTGATTTAAGAGTCATTGCCAG , CM000675.1:g.23905711_23905712insCAATTTGATTTCTGACACTTCATATCAAATTGTCAGTTGCTGATTTAAGAGTCATTGCCAG GRCh37
NC_000013.9:g.22803711_22803712insCAATTTGATTTCTGACACTTCATATCAAATTGTCAGTTGCTGATTTAAGAGTCATTGCCAG NCBI36
NG_012342.1:g.107130_107131insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-19458_2186-19457insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000508399.1:n.2186-19458_2186-19457insCTGGCAATGACTCTTAA...
ENST00000682944.1:c.12330_12331insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000507173.1:p.Ser4124Ter
ENST00000683210.1:c.2185+22212_2185+22213insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000506739.1:n.2185+22212_2185+22213insCTGGCAATGACTCTTAA...
ENST00000683270.1:c.6446-2089_6446-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000507624.1:n.6446-2089_6446-2088insCTGGCAATGACTCTTAAAT...
ENST00000683367.1:c.2177-2089_2177-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000507780.1:n.2177-2089_2177-2088insCTGGCAATGACTCTTAAAT...
ENST00000683489.1:c.2292-1621_2292-1620insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000508403.1:n.2292-1621_2292-1620insCTGGCAATGACTCTTAAAT...
ENST00000683680.1:c.2319-1621_2319-1620insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000507223.1:n.2319-1621_2319-1620insCTGGCAATGACTCTTAAAT...
ENST00000684163.1:c.2204-2089_2204-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000508262.1:n.2204-2089_2204-2088insCTGGCAATGACTCTTAAAT...
ENST00000684196.1:n.4543-2089_4543-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG
ENST00000684325.1:c.2186-9899_2186-9898insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000508121.1:n.2186-9899_2186-9898insCTGGCAATGACTCTTAAAT...
ENST00000684385.1:c.2221-2089_2221-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000507855.1:n.2221-2089_2221-2088insCTGGCAATGACTCTTAAAT...
ENST00000684497.1:c.2186-8929_2186-8928insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000507057.1:n.2186-8929_2186-8928insCTGGCAATGACTCTTAAAT...
ENST00000382292.9:c.12303_12304insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG MANE Select ENSP00000371729.3:p.Ser4115Ter
ENST00000423156.2:c.2186-2089_2186-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000390925.2:n.2186-2089_2186-2088insCTGGCAATGACTCTTAAAT...
ENST00000455470.6:c.2432-2089_2432-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000406565.2:n.2432-2089_2432-2088insCTGGCAATGACTCTTAAAT...
ENST00000382292.7:c.12303_12304insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000371729.3:p.Ser4115Ter
ENST00000382298.7:c.12303_12304insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000371735.3:p.Ser4115Ter
ENST00000402364.1:c.10053_10054insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000385844.1:p.Ser3365Ter
ENST00000423156.1:c.1058-2089_1058-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG ENSP00000390925.1:n.1058-2089_1058-2088insCTGGCAATGACTCTTAAAT...
ENST00000455470.5:c.2130-2089_2130-2088insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG
NM_001278055.1:c.11862_11863insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG NP_001264984.1:p.Ser3968Ter
NM_014363.5:c.12303_12304insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG NP_055178.3:p.Ser4115Ter
XM_005266338.1:c.12330_12331insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_005266395.1:p.Ser4124Ter
XM_011535038.1:c.12354_12355insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_011533340.1:p.Ser4132Ter
XM_011535039.1:c.12321_12322insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_011533341.1:p.Ser4121Ter
XM_005266338.2:c.12330_12331insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_005266395.1:p.Ser4124Ter
XM_011535039.2:c.12321_12322insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_011533341.1:p.Ser4121Ter
XM_017020539.1:c.12294_12295insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_016876028.1:p.Ser4112Ter
XM_024449337.1:c.12330_12331insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG XP_024305105.1:p.Ser4124Ter
NM_014363.6:c.12303_12304insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG MANE Select NP_055178.3:p.Ser4115Ter
NM_001278055.2:c.11862_11863insCTGGCAATGACTCTTAAATCAGCAACTGACAATTTGATATGAAGTGTCAGAAATCAAATTG NP_001264984.1:p.Ser3968Ter