Canonical Allele Identifier: CA6912063
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs780802745

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23358442G>A , CM000675.2:g.23358442G>A GRCh38
NC_000013.10:g.23932581G>A , CM000675.1:g.23932581G>A GRCh37
NC_000013.9:g.22830581G>A NCBI36
NG_012342.1:g.80261C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.497C>T ENSP00000508399.1:p.Pro166Leu
ENST00000682944.1:c.497C>T ENSP00000507173.1:p.Pro166Leu
ENST00000683154.1:n.635C>T
ENST00000683210.1:c.497C>T ENSP00000506739.1:p.Pro166Leu
ENST00000683270.1:c.488C>T ENSP00000507624.1:p.Pro163Leu
ENST00000683367.1:c.488C>T ENSP00000507780.1:p.Pro163Leu
ENST00000683489.1:c.497C>T ENSP00000508403.1:p.Pro166Leu
ENST00000683680.1:c.497C>T ENSP00000507223.1:p.Pro166Leu
ENST00000684163.1:c.488C>T ENSP00000508262.1:p.Pro163Leu
ENST00000684196.1:n.2854C>T
ENST00000684325.1:c.497C>T ENSP00000508121.1:p.Pro166Leu
ENST00000684385.1:c.497C>T ENSP00000507855.1:p.Pro166Leu
ENST00000684497.1:c.497C>T ENSP00000507057.1:p.Pro166Leu
ENST00000382292.9:c.497C>T MANE Select ENSP00000371729.3:p.Pro166Leu
ENST00000423156.2:c.497C>T ENSP00000390925.2:p.Pro166Leu
ENST00000455470.6:c.497C>T ENSP00000406565.2:p.Pro166Leu
ENST00000382292.7:c.497C>T ENSP00000371729.3:p.Pro166Leu
ENST00000382298.7:c.497C>T ENSP00000371735.3:p.Pro166Leu
ENST00000402364.1:c.-1754C>T ENSP00000385844.1:n.-1754C>T
ENST00000455470.5:c.195C>T
NM_001278055.1:c.56C>T NP_001264984.1:p.Pro19Leu
NM_014363.5:c.497C>T NP_055178.3:p.Pro166Leu
XM_005266338.1:c.497C>T XP_005266395.1:p.Pro166Leu
XM_011535038.1:c.521C>T XP_011533340.1:p.Pro174Leu
XM_011535039.1:c.488C>T XP_011533341.1:p.Pro163Leu
XM_005266338.2:c.497C>T XP_005266395.1:p.Pro166Leu
XM_011535039.2:c.488C>T XP_011533341.1:p.Pro163Leu
XM_017020539.1:c.488C>T XP_016876028.1:p.Pro163Leu
XM_024449337.1:c.497C>T XP_024305105.1:p.Pro166Leu
NM_014363.6:c.497C>T MANE Select NP_055178.3:p.Pro166Leu
NM_001278055.2:c.56C>T NP_001264984.1:p.Pro19Leu