Canonical Allele Identifier: CA2622331284
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23355542_23355545del , CM000675.2:g.23355542_23355545del GRCh38
NC_000013.10:g.23929681_23929684del , CM000675.1:g.23929681_23929684del GRCh37
NC_000013.9:g.22827681_22827684del NCBI36
NG_012342.1:g.83161_83164del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.1070_1073del ENSP00000508399.1:p.Ser357ThrfsTer14
ENST00000682944.1:c.1070_1073del ENSP00000507173.1:p.Ser357ThrfsTer14
ENST00000683154.1:n.1208_1211del
ENST00000683210.1:c.1070_1073del ENSP00000506739.1:p.Ser357ThrfsTer14
ENST00000683270.1:c.1061_1064del ENSP00000507624.1:p.Ser354ThrfsTer14
ENST00000683367.1:c.1061_1064del ENSP00000507780.1:p.Ser354ThrfsTer14
ENST00000683489.1:c.1070_1073del ENSP00000508403.1:p.Ser357ThrfsTer14
ENST00000683680.1:c.1070_1073del ENSP00000507223.1:p.Ser357ThrfsTer14
ENST00000684163.1:c.1061_1064del ENSP00000508262.1:p.Ser354ThrfsTer14
ENST00000684196.1:n.3427_3430del
ENST00000684325.1:c.1070_1073del ENSP00000508121.1:p.Ser357ThrfsTer14
ENST00000684385.1:c.1070_1073del ENSP00000507855.1:p.Ser357ThrfsTer14
ENST00000684497.1:c.1070_1073del ENSP00000507057.1:p.Ser357ThrfsTer14
ENST00000382292.9:c.1070_1073del MANE Select ENSP00000371729.3:p.Ser357ThrfsTer14
ENST00000423156.2:c.1070_1073del ENSP00000390925.2:p.Ser357ThrfsTer14
ENST00000455470.6:c.1070_1073del ENSP00000406565.2:p.Ser357ThrfsTer14
ENST00000382292.7:c.1070_1073del ENSP00000371729.3:p.Ser357ThrfsTer14
ENST00000382298.7:c.1070_1073del ENSP00000371735.3:p.Ser357ThrfsTer14
ENST00000402364.1:c.-1181_-1178del ENSP00000385844.1:n.-1181_-1178del
ENST00000455470.5:c.768_771del
NM_001278055.1:c.629_632del NP_001264984.1:p.Ser210ThrfsTer14
NM_014363.5:c.1070_1073del NP_055178.3:p.Ser357ThrfsTer14
XM_005266338.1:c.1070_1073del XP_005266395.1:p.Ser357ThrfsTer14
XM_011535038.1:c.1094_1097del XP_011533340.1:p.Ser365ThrfsTer14
XM_011535039.1:c.1061_1064del XP_011533341.1:p.Ser354ThrfsTer14
XM_005266338.2:c.1070_1073del XP_005266395.1:p.Ser357ThrfsTer14
XM_011535039.2:c.1061_1064del XP_011533341.1:p.Ser354ThrfsTer14
XM_017020539.1:c.1061_1064del XP_016876028.1:p.Ser354ThrfsTer14
XM_024449337.1:c.1070_1073del XP_024305105.1:p.Ser357ThrfsTer14
NM_014363.6:c.1070_1073del MANE Select NP_055178.3:p.Ser357ThrfsTer14
NM_001278055.2:c.629_632del NP_001264984.1:p.Ser210ThrfsTer14