Canonical Allele Identifier: CA2622331281
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23355422dup , CM000675.2:g.23355422dup GRCh38
NC_000013.10:g.23929561dup , CM000675.1:g.23929561dup GRCh37
NC_000013.9:g.22827561dup NCBI36
NG_012342.1:g.83281dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.1190dup ENSP00000508399.1:p.Ser397ArgfsTer9
ENST00000682944.1:c.1190dup ENSP00000507173.1:p.Ser397ArgfsTer9
ENST00000683154.1:n.1328dup
ENST00000683210.1:c.1190dup ENSP00000506739.1:p.Ser397ArgfsTer9
ENST00000683270.1:c.1181dup ENSP00000507624.1:p.Ser394ArgfsTer9
ENST00000683367.1:c.1181dup ENSP00000507780.1:p.Ser394ArgfsTer9
ENST00000683489.1:c.1190dup ENSP00000508403.1:p.Ser397ArgfsTer9
ENST00000683680.1:c.1190dup ENSP00000507223.1:p.Ser397ArgfsTer9
ENST00000684163.1:c.1181dup ENSP00000508262.1:p.Ser394ArgfsTer9
ENST00000684196.1:n.3547dup
ENST00000684325.1:c.1190dup ENSP00000508121.1:p.Ser397ArgfsTer9
ENST00000684385.1:c.1190dup ENSP00000507855.1:p.Ser397ArgfsTer9
ENST00000684497.1:c.1190dup ENSP00000507057.1:p.Ser397ArgfsTer9
ENST00000382292.9:c.1190dup MANE Select ENSP00000371729.3:p.Ser397ArgfsTer9
ENST00000423156.2:c.1190dup ENSP00000390925.2:p.Ser397ArgfsTer9
ENST00000455470.6:c.1190dup ENSP00000406565.2:p.Ser397ArgfsTer9
ENST00000382292.7:c.1190dup ENSP00000371729.3:p.Ser397ArgfsTer9
ENST00000382298.7:c.1190dup ENSP00000371735.3:p.Ser397ArgfsTer9
ENST00000402364.1:c.-1061dup ENSP00000385844.1:n.-1061dup
ENST00000423156.1:c.62dup ENSP00000390925.1:p.Ser21ArgfsTer9
ENST00000455470.5:c.888dup
NM_001278055.1:c.749dup NP_001264984.1:p.Ser250ArgfsTer9
NM_014363.5:c.1190dup NP_055178.3:p.Ser397ArgfsTer9
XM_005266338.1:c.1190dup XP_005266395.1:p.Ser397ArgfsTer9
XM_011535038.1:c.1214dup XP_011533340.1:p.Ser405ArgfsTer9
XM_011535039.1:c.1181dup XP_011533341.1:p.Ser394ArgfsTer9
XM_005266338.2:c.1190dup XP_005266395.1:p.Ser397ArgfsTer9
XM_011535039.2:c.1181dup XP_011533341.1:p.Ser394ArgfsTer9
XM_017020539.1:c.1181dup XP_016876028.1:p.Ser394ArgfsTer9
XM_024449337.1:c.1190dup XP_024305105.1:p.Ser397ArgfsTer9
NM_014363.6:c.1190dup MANE Select NP_055178.3:p.Ser397ArgfsTer9
NM_001278055.2:c.749dup NP_001264984.1:p.Ser250ArgfsTer9