Canonical Allele Identifier: CA2622329003
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23336137del , CM000675.2:g.23336137del GRCh38
NC_000013.10:g.23910276del , CM000675.1:g.23910276del GRCh37
NC_000013.9:g.22808276del NCBI36
NG_012342.1:g.102568del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+17650del ENSP00000508399.1:n.2185+17650del
ENST00000682944.1:c.7768del ENSP00000507173.1:p.Ala2590ProfsTer?
ENST00000683210.1:c.2185+17650del ENSP00000506739.1:n.2185+17650del
ENST00000683270.1:c.6445+1287del ENSP00000507624.1:n.6445+1287del
ENST00000683367.1:c.2177-6651del ENSP00000507780.1:n.2177-6651del
ENST00000683489.1:c.2291+5450del ENSP00000508403.1:n.2291+5450del
ENST00000683680.1:c.2318+5450del ENSP00000507223.1:n.2318+5450del
ENST00000684163.1:c.2204-6651del ENSP00000508262.1:n.2204-6651del
ENST00000684196.1:n.4543-6651del
ENST00000684325.1:c.2186-14461del ENSP00000508121.1:n.2186-14461del
ENST00000684385.1:c.2221-6651del ENSP00000507855.1:n.2221-6651del
ENST00000684497.1:c.2186-13491del ENSP00000507057.1:n.2186-13491del
ENST00000382292.9:c.7741del MANE Select ENSP00000371729.3:p.Ala2581ProfsTer?
ENST00000423156.2:c.2186-6651del ENSP00000390925.2:n.2186-6651del
ENST00000455470.6:c.2431+5310del ENSP00000406565.2:n.2431+5310del
ENST00000382292.7:c.7741del ENSP00000371729.3:p.Ala2581ProfsTer?
ENST00000382298.7:c.7741del ENSP00000371735.3:p.Ala2581ProfsTer?
ENST00000402364.1:c.5491del ENSP00000385844.1:p.Ala1831ProfsTer?
ENST00000423156.1:c.1058-6651del ENSP00000390925.1:n.1058-6651del
ENST00000455470.5:c.2129+5310del
NM_001278055.1:c.7300del NP_001264984.1:p.Ala2434ProfsTer?
NM_014363.5:c.7741del NP_055178.3:p.Ala2581ProfsTer?
XM_005266338.1:c.7768del XP_005266395.1:p.Ala2590ProfsTer?
XM_011535038.1:c.7792del XP_011533340.1:p.Ala2598ProfsTer?
XM_011535039.1:c.7759del XP_011533341.1:p.Ala2587ProfsTer?
XM_005266338.2:c.7768del XP_005266395.1:p.Ala2590ProfsTer?
XM_011535039.2:c.7759del XP_011533341.1:p.Ala2587ProfsTer?
XM_017020539.1:c.7732del XP_016876028.1:p.Ala2578ProfsTer?
XM_024449337.1:c.7768del XP_024305105.1:p.Ala2590ProfsTer?
NM_014363.6:c.7741del MANE Select NP_055178.3:p.Ala2581ProfsTer?
NM_001278055.2:c.7300del NP_001264984.1:p.Ala2434ProfsTer?