Canonical Allele Identifier: CA2559427720
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23339817_23339818insGAACATAACTAGGTTAGGAGAATCTTTAAAAAGGGGAGAAG , CM000675.2:g.23339817_23339818insGAACATAACTAGGTTAGGAGAATCTTTAAAAAGGGGAGAAG GRCh38
NC_000013.10:g.23913956_23913957insGAACATAACTAGGTTAGGAGAATCTTTAAAAAGGGGAGAAG , CM000675.1:g.23913956_23913957insGAACATAACTAGGTTAGGAGAATCTTTAAAAAGGGGAGAAG GRCh37
NC_000013.9:g.22811956_22811957insGAACATAACTAGGTTAGGAGAATCTTTAAAAAGGGGAGAAG NCBI36
NG_012342.1:g.98885_98886insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+13967_2185+13968insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000508399.1:n.2185+13967_2185+13968insCTTCTCCCCTTTTTAAA...
ENST00000682944.1:c.4085_4086insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000507173.1:p.Lys1362AsnfsTer6
ENST00000683210.1:c.2185+13967_2185+13968insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000506739.1:n.2185+13967_2185+13968insCTTCTCCCCTTTTTAAA...
ENST00000683270.1:c.4049_4050insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000507624.1:p.Lys1350AsnfsTer6
ENST00000683367.1:c.2177-10334_2177-10333insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000507780.1:n.2177-10334_2177-10333insCTTCTCCCCTTTTTAAA...
ENST00000683489.1:c.2291+1767_2291+1768insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000508403.1:n.2291+1767_2291+1768insCTTCTCCCCTTTTTAAAGA...
ENST00000683680.1:c.2318+1767_2318+1768insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000507223.1:n.2318+1767_2318+1768insCTTCTCCCCTTTTTAAAGA...
ENST00000684163.1:c.2203+6993_2203+6994insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000508262.1:n.2203+6993_2203+6994insCTTCTCCCCTTTTTAAAGA...
ENST00000684196.1:n.4543-10334_4543-10333insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC
ENST00000684325.1:c.2185+13967_2185+13968insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000508121.1:n.2185+13967_2185+13968insCTTCTCCCCTTTTTAAA...
ENST00000684385.1:c.2220+6993_2220+6994insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000507855.1:n.2220+6993_2220+6994insCTTCTCCCCTTTTTAAAGA...
ENST00000684497.1:c.2185+13967_2185+13968insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000507057.1:n.2185+13967_2185+13968insCTTCTCCCCTTTTTAAA...
ENST00000382292.9:c.4058_4059insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC MANE Select ENSP00000371729.3:p.Lys1353AsnfsTer6
ENST00000423156.2:c.2186-10334_2186-10333insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000390925.2:n.2186-10334_2186-10333insCTTCTCCCCTTTTTAAA...
ENST00000455470.6:c.2431+1627_2431+1628insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000406565.2:n.2431+1627_2431+1628insCTTCTCCCCTTTTTAAAGA...
ENST00000382292.7:c.4058_4059insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000371729.3:p.Lys1353AsnfsTer6
ENST00000382298.7:c.4058_4059insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000371735.3:p.Lys1353AsnfsTer6
ENST00000402364.1:c.1808_1809insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000385844.1:p.Lys603AsnfsTer6
ENST00000423156.1:c.1058-10334_1058-10333insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC ENSP00000390925.1:n.1058-10334_1058-10333insCTTCTCCCCTTTTTAAA...
ENST00000455470.5:c.2129+1627_2129+1628insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC
NM_001278055.1:c.3617_3618insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC NP_001264984.1:p.Lys1206AsnfsTer6
NM_014363.5:c.4058_4059insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC NP_055178.3:p.Lys1353AsnfsTer6
XM_005266338.1:c.4085_4086insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_005266395.1:p.Lys1362AsnfsTer6
XM_011535038.1:c.4109_4110insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_011533340.1:p.Lys1370AsnfsTer6
XM_011535039.1:c.4076_4077insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_011533341.1:p.Lys1359AsnfsTer6
XM_005266338.2:c.4085_4086insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_005266395.1:p.Lys1362AsnfsTer6
XM_011535039.2:c.4076_4077insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_011533341.1:p.Lys1359AsnfsTer6
XM_017020539.1:c.4049_4050insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_016876028.1:p.Lys1350AsnfsTer6
XM_024449337.1:c.4085_4086insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC XP_024305105.1:p.Lys1362AsnfsTer6
NM_014363.6:c.4058_4059insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC MANE Select NP_055178.3:p.Lys1353AsnfsTer6
NM_001278055.2:c.3617_3618insCTTCTCCCCTTTTTAAAGATTCTCCTAACCTAGTTATGTTC NP_001264984.1:p.Lys1206AsnfsTer6