Canonical Allele Identifier: CA2078628482
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330735A= , CM000675.2:g.23330735A= GRCh38
NC_000013.10:g.23904874A= , CM000675.1:g.23904874A= GRCh37
NC_000013.9:g.22802874A= NCBI36
NG_012342.1:g.107968T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-18620T= ENSP00000508399.1:n.2186-18620T=
ENST00000682944.1:c.13168T= ENSP00000507173.1:p.Ser4390=
ENST00000683210.1:c.2185+23050T= ENSP00000506739.1:n.2185+23050T=
ENST00000683270.1:c.6446-1251T= ENSP00000507624.1:n.6446-1251T=
ENST00000683367.1:c.2177-1251T= ENSP00000507780.1:n.2177-1251T=
ENST00000683489.1:c.2292-783T= ENSP00000508403.1:n.2292-783T=
ENST00000683680.1:c.2319-783T= ENSP00000507223.1:n.2319-783T=
ENST00000684163.1:c.2204-1251T= ENSP00000508262.1:n.2204-1251T=
ENST00000684196.1:n.4543-1251T=
ENST00000684325.1:c.2186-9061T= ENSP00000508121.1:n.2186-9061T=
ENST00000684385.1:c.2221-1251T= ENSP00000507855.1:n.2221-1251T=
ENST00000684497.1:c.2186-8091T= ENSP00000507057.1:n.2186-8091T=
ENST00000382292.9:c.13141T= MANE Select ENSP00000371729.3:p.Ser4381=
ENST00000423156.2:c.2186-1251T= ENSP00000390925.2:n.2186-1251T=
ENST00000455470.6:c.2432-1251T= ENSP00000406565.2:n.2432-1251T=
ENST00000382292.7:c.13141T= ENSP00000371729.3:p.Ser4381=
ENST00000382298.7:c.13141T= ENSP00000371735.3:p.Ser4381=
ENST00000402364.1:c.10891T= ENSP00000385844.1:p.Ser3631=
ENST00000423156.1:c.1058-1251T= ENSP00000390925.1:n.1058-1251T=
ENST00000455470.5:c.2130-1251T=
NM_001278055.1:c.12700T= NP_001264984.1:p.Ser4234=
NM_014363.5:c.13141T= NP_055178.3:p.Ser4381=
XM_005266338.1:c.13168T= XP_005266395.1:p.Ser4390=
XM_011535038.1:c.13192T= XP_011533340.1:p.Ser4398=
XM_011535039.1:c.13159T= XP_011533341.1:p.Ser4387=
XM_005266338.2:c.13168T= XP_005266395.1:p.Ser4390=
XM_011535039.2:c.13159T= XP_011533341.1:p.Ser4387=
XM_017020539.1:c.13132T= XP_016876028.1:p.Ser4378=
XM_024449337.1:c.13168T= XP_024305105.1:p.Ser4390=
NM_014363.6:c.13141T= MANE Select NP_055178.3:p.Ser4381=
NM_001278055.2:c.12700T= NP_001264984.1:p.Ser4234=