Canonical Allele Identifier: CA2078628804
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330926G= , CM000675.2:g.23330926G= GRCh38
NC_000013.10:g.23905065G= , CM000675.1:g.23905065G= GRCh37
NC_000013.9:g.22803065G= NCBI36
NG_012342.1:g.107777C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-18811C= ENSP00000508399.1:n.2186-18811C=
ENST00000682944.1:c.12977C= ENSP00000507173.1:p.Ala4326=
ENST00000683210.1:c.2185+22859C= ENSP00000506739.1:n.2185+22859C=
ENST00000683270.1:c.6446-1442C= ENSP00000507624.1:n.6446-1442C=
ENST00000683367.1:c.2177-1442C= ENSP00000507780.1:n.2177-1442C=
ENST00000683489.1:c.2292-974C= ENSP00000508403.1:n.2292-974C=
ENST00000683680.1:c.2319-974C= ENSP00000507223.1:n.2319-974C=
ENST00000684163.1:c.2204-1442C= ENSP00000508262.1:n.2204-1442C=
ENST00000684196.1:n.4543-1442C=
ENST00000684325.1:c.2186-9252C= ENSP00000508121.1:n.2186-9252C=
ENST00000684385.1:c.2221-1442C= ENSP00000507855.1:n.2221-1442C=
ENST00000684497.1:c.2186-8282C= ENSP00000507057.1:n.2186-8282C=
ENST00000382292.9:c.12950C= MANE Select ENSP00000371729.3:p.Ala4317=
ENST00000423156.2:c.2186-1442C= ENSP00000390925.2:n.2186-1442C=
ENST00000455470.6:c.2432-1442C= ENSP00000406565.2:n.2432-1442C=
ENST00000382292.7:c.12950C= ENSP00000371729.3:p.Ala4317=
ENST00000382298.7:c.12950C= ENSP00000371735.3:p.Ala4317=
ENST00000402364.1:c.10700C= ENSP00000385844.1:p.Ala3567=
ENST00000423156.1:c.1058-1442C= ENSP00000390925.1:n.1058-1442C=
ENST00000455470.5:c.2130-1442C=
NM_001278055.1:c.12509C= NP_001264984.1:p.Ala4170=
NM_014363.5:c.12950C= NP_055178.3:p.Ala4317=
XM_005266338.1:c.12977C= XP_005266395.1:p.Ala4326=
XM_011535038.1:c.13001C= XP_011533340.1:p.Ala4334=
XM_011535039.1:c.12968C= XP_011533341.1:p.Ala4323=
XM_005266338.2:c.12977C= XP_005266395.1:p.Ala4326=
XM_011535039.2:c.12968C= XP_011533341.1:p.Ala4323=
XM_017020539.1:c.12941C= XP_016876028.1:p.Ala4314=
XM_024449337.1:c.12977C= XP_024305105.1:p.Ala4326=
NM_014363.6:c.12950C= MANE Select NP_055178.3:p.Ala4317=
NM_001278055.2:c.12509C= NP_001264984.1:p.Ala4170=