Canonical Allele Identifier: CA2078628825
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330943T= , CM000675.2:g.23330943T= GRCh38
NC_000013.10:g.23905082T= , CM000675.1:g.23905082T= GRCh37
NC_000013.9:g.22803082T= NCBI36
NG_012342.1:g.107760A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-18828A= ENSP00000508399.1:n.2186-18828A=
ENST00000682944.1:c.12960A= ENSP00000507173.1:p.Thr4320=
ENST00000683210.1:c.2185+22842A= ENSP00000506739.1:n.2185+22842A=
ENST00000683270.1:c.6446-1459A= ENSP00000507624.1:n.6446-1459A=
ENST00000683367.1:c.2177-1459A= ENSP00000507780.1:n.2177-1459A=
ENST00000683489.1:c.2292-991A= ENSP00000508403.1:n.2292-991A=
ENST00000683680.1:c.2319-991A= ENSP00000507223.1:n.2319-991A=
ENST00000684163.1:c.2204-1459A= ENSP00000508262.1:n.2204-1459A=
ENST00000684196.1:n.4543-1459A=
ENST00000684325.1:c.2186-9269A= ENSP00000508121.1:n.2186-9269A=
ENST00000684385.1:c.2221-1459A= ENSP00000507855.1:n.2221-1459A=
ENST00000684497.1:c.2186-8299A= ENSP00000507057.1:n.2186-8299A=
ENST00000382292.9:c.12933A= MANE Select ENSP00000371729.3:p.Thr4311=
ENST00000423156.2:c.2186-1459A= ENSP00000390925.2:n.2186-1459A=
ENST00000455470.6:c.2432-1459A= ENSP00000406565.2:n.2432-1459A=
ENST00000382292.7:c.12933A= ENSP00000371729.3:p.Thr4311=
ENST00000382298.7:c.12933A= ENSP00000371735.3:p.Thr4311=
ENST00000402364.1:c.10683A= ENSP00000385844.1:p.Thr3561=
ENST00000423156.1:c.1058-1459A= ENSP00000390925.1:n.1058-1459A=
ENST00000455470.5:c.2130-1459A=
NM_001278055.1:c.12492A= NP_001264984.1:p.Thr4164=
NM_014363.5:c.12933A= NP_055178.3:p.Thr4311=
XM_005266338.1:c.12960A= XP_005266395.1:p.Thr4320=
XM_011535038.1:c.12984A= XP_011533340.1:p.Thr4328=
XM_011535039.1:c.12951A= XP_011533341.1:p.Thr4317=
XM_005266338.2:c.12960A= XP_005266395.1:p.Thr4320=
XM_011535039.2:c.12951A= XP_011533341.1:p.Thr4317=
XM_017020539.1:c.12924A= XP_016876028.1:p.Thr4308=
XM_024449337.1:c.12960A= XP_024305105.1:p.Thr4320=
NM_014363.6:c.12933A= MANE Select NP_055178.3:p.Thr4311=
NM_001278055.2:c.12492A= NP_001264984.1:p.Thr4164=