Canonical Allele Identifier: CA2622328865
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330990del , CM000675.2:g.23330990del GRCh38
NC_000013.10:g.23905129del , CM000675.1:g.23905129del GRCh37
NC_000013.9:g.22803129del NCBI36
NG_012342.1:g.107717del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-18871del ENSP00000508399.1:n.2186-18871del
ENST00000682944.1:c.12917del ENSP00000507173.1:p.Lys4306SerfsTer11
ENST00000683210.1:c.2185+22799del ENSP00000506739.1:n.2185+22799del
ENST00000683270.1:c.6446-1502del ENSP00000507624.1:n.6446-1502del
ENST00000683367.1:c.2177-1502del ENSP00000507780.1:n.2177-1502del
ENST00000683489.1:c.2292-1034del ENSP00000508403.1:n.2292-1034del
ENST00000683680.1:c.2319-1034del ENSP00000507223.1:n.2319-1034del
ENST00000684163.1:c.2204-1502del ENSP00000508262.1:n.2204-1502del
ENST00000684196.1:n.4543-1502del
ENST00000684325.1:c.2186-9312del ENSP00000508121.1:n.2186-9312del
ENST00000684385.1:c.2221-1502del ENSP00000507855.1:n.2221-1502del
ENST00000684497.1:c.2186-8342del ENSP00000507057.1:n.2186-8342del
ENST00000382292.9:c.12890del MANE Select ENSP00000371729.3:p.Lys4297SerfsTer11
ENST00000423156.2:c.2186-1502del ENSP00000390925.2:n.2186-1502del
ENST00000455470.6:c.2432-1502del ENSP00000406565.2:n.2432-1502del
ENST00000382292.7:c.12890del ENSP00000371729.3:p.Lys4297SerfsTer11
ENST00000382298.7:c.12890del ENSP00000371735.3:p.Lys4297SerfsTer11
ENST00000402364.1:c.10640del ENSP00000385844.1:p.Lys3547SerfsTer11
ENST00000423156.1:c.1058-1502del ENSP00000390925.1:n.1058-1502del
ENST00000455470.5:c.2130-1502del
NM_001278055.1:c.12449del NP_001264984.1:p.Lys4150SerfsTer11
NM_014363.5:c.12890del NP_055178.3:p.Lys4297SerfsTer11
XM_005266338.1:c.12917del XP_005266395.1:p.Lys4306SerfsTer11
XM_011535038.1:c.12941del XP_011533340.1:p.Lys4314SerfsTer11
XM_011535039.1:c.12908del XP_011533341.1:p.Lys4303SerfsTer11
XM_005266338.2:c.12917del XP_005266395.1:p.Lys4306SerfsTer11
XM_011535039.2:c.12908del XP_011533341.1:p.Lys4303SerfsTer11
XM_017020539.1:c.12881del XP_016876028.1:p.Lys4294SerfsTer11
XM_024449337.1:c.12917del XP_024305105.1:p.Lys4306SerfsTer11
NM_014363.6:c.12890del MANE Select NP_055178.3:p.Lys4297SerfsTer11
NM_001278055.2:c.12449del NP_001264984.1:p.Lys4150SerfsTer11