Canonical Allele Identifier: CA2078628410
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337970T= , CM000675.2:g.23337970T= GRCh38
NC_000013.10:g.23912109T= , CM000675.1:g.23912109T= GRCh37
NC_000013.9:g.22810109T= NCBI36
NG_012342.1:g.100733A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+15815A= ENSP00000508399.1:n.2185+15815A=
ENST00000682944.1:c.5933A= ENSP00000507173.1:p.His1978=
ENST00000683210.1:c.2185+15815A= ENSP00000506739.1:n.2185+15815A=
ENST00000683270.1:c.5897A= ENSP00000507624.1:p.His1966=
ENST00000683367.1:c.2177-8486A= ENSP00000507780.1:n.2177-8486A=
ENST00000683489.1:c.2291+3615A= ENSP00000508403.1:n.2291+3615A=
ENST00000683680.1:c.2318+3615A= ENSP00000507223.1:n.2318+3615A=
ENST00000684163.1:c.2204-8486A= ENSP00000508262.1:n.2204-8486A=
ENST00000684196.1:n.4543-8486A=
ENST00000684325.1:c.2185+15815A= ENSP00000508121.1:n.2185+15815A=
ENST00000684385.1:c.2221-8486A= ENSP00000507855.1:n.2221-8486A=
ENST00000684497.1:c.2186-15326A= ENSP00000507057.1:n.2186-15326A=
ENST00000382292.9:c.5906A= MANE Select ENSP00000371729.3:p.His1969=
ENST00000423156.2:c.2186-8486A= ENSP00000390925.2:n.2186-8486A=
ENST00000455470.6:c.2431+3475A= ENSP00000406565.2:n.2431+3475A=
ENST00000382292.7:c.5906A= ENSP00000371729.3:p.His1969=
ENST00000382298.7:c.5906A= ENSP00000371735.3:p.His1969=
ENST00000402364.1:c.3656A= ENSP00000385844.1:p.His1219=
ENST00000423156.1:c.1058-8486A= ENSP00000390925.1:n.1058-8486A=
ENST00000455470.5:c.2129+3475A=
NM_001278055.1:c.5465A= NP_001264984.1:p.His1822=
NM_014363.5:c.5906A= NP_055178.3:p.His1969=
XM_005266338.1:c.5933A= XP_005266395.1:p.His1978=
XM_011535038.1:c.5957A= XP_011533340.1:p.His1986=
XM_011535039.1:c.5924A= XP_011533341.1:p.His1975=
XM_005266338.2:c.5933A= XP_005266395.1:p.His1978=
XM_011535039.2:c.5924A= XP_011533341.1:p.His1975=
XM_017020539.1:c.5897A= XP_016876028.1:p.His1966=
XM_024449337.1:c.5933A= XP_024305105.1:p.His1978=
NM_014363.6:c.5906A= MANE Select NP_055178.3:p.His1969=
NM_001278055.2:c.5465A= NP_001264984.1:p.His1822=