Canonical Allele Identifier: CA2078631907
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23332740T= , CM000675.2:g.23332740T= GRCh38
NC_000013.10:g.23906879T= , CM000675.1:g.23906879T= GRCh37
NC_000013.9:g.22804879T= NCBI36
NG_012342.1:g.105963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-20625A= ENSP00000508399.1:n.2186-20625A=
ENST00000682944.1:c.11163A= ENSP00000507173.1:p.Thr3721=
ENST00000683210.1:c.2185+21045A= ENSP00000506739.1:n.2185+21045A=
ENST00000683270.1:c.6446-3256A= ENSP00000507624.1:n.6446-3256A=
ENST00000683367.1:c.2177-3256A= ENSP00000507780.1:n.2177-3256A=
ENST00000683489.1:c.2292-2788A= ENSP00000508403.1:n.2292-2788A=
ENST00000683680.1:c.2319-2788A= ENSP00000507223.1:n.2319-2788A=
ENST00000684163.1:c.2204-3256A= ENSP00000508262.1:n.2204-3256A=
ENST00000684196.1:n.4543-3256A=
ENST00000684325.1:c.2186-11066A= ENSP00000508121.1:n.2186-11066A=
ENST00000684385.1:c.2221-3256A= ENSP00000507855.1:n.2221-3256A=
ENST00000684497.1:c.2186-10096A= ENSP00000507057.1:n.2186-10096A=
ENST00000382292.9:c.11136A= MANE Select ENSP00000371729.3:p.Thr3712=
ENST00000423156.2:c.2186-3256A= ENSP00000390925.2:n.2186-3256A=
ENST00000455470.6:c.2432-3256A= ENSP00000406565.2:n.2432-3256A=
ENST00000382292.7:c.11136A= ENSP00000371729.3:p.Thr3712=
ENST00000382298.7:c.11136A= ENSP00000371735.3:p.Thr3712=
ENST00000402364.1:c.8886A= ENSP00000385844.1:p.Thr2962=
ENST00000423156.1:c.1058-3256A= ENSP00000390925.1:n.1058-3256A=
ENST00000455470.5:c.2130-3256A=
NM_001278055.1:c.10695A= NP_001264984.1:p.Thr3565=
NM_014363.5:c.11136A= NP_055178.3:p.Thr3712=
XM_005266338.1:c.11163A= XP_005266395.1:p.Thr3721=
XM_011535038.1:c.11187A= XP_011533340.1:p.Thr3729=
XM_011535039.1:c.11154A= XP_011533341.1:p.Thr3718=
XM_005266338.2:c.11163A= XP_005266395.1:p.Thr3721=
XM_011535039.2:c.11154A= XP_011533341.1:p.Thr3718=
XM_017020539.1:c.11127A= XP_016876028.1:p.Thr3709=
XM_024449337.1:c.11163A= XP_024305105.1:p.Thr3721=
NM_014363.6:c.11136A= MANE Select NP_055178.3:p.Thr3712=
NM_001278055.2:c.10695A= NP_001264984.1:p.Thr3565=