Canonical Allele Identifier: CA387554600
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs1593160953

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23375196G>C , CM000675.2:g.23375196G>C GRCh38
NC_000013.10:g.23949335G>C , CM000675.1:g.23949335G>C GRCh37
NC_000013.9:g.22847335G>C NCBI36
NG_012342.1:g.63507C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682244.1:n.667C>G
ENST00000682547.1:c.131C>G ENSP00000507735.1:p.Ala44Gly
ENST00000682775.1:c.94C>G ENSP00000508399.1:p.Arg32Gly
ENST00000682944.1:c.94C>G ENSP00000507173.1:p.Arg32Gly
ENST00000683154.1:n.232C>G
ENST00000683210.1:c.94C>G ENSP00000506739.1:p.Arg32Gly
ENST00000683270.1:c.85C>G ENSP00000507624.1:p.Arg29Gly
ENST00000683367.1:c.85C>G ENSP00000507780.1:p.Arg29Gly
ENST00000683489.1:c.94C>G ENSP00000508403.1:p.Arg32Gly
ENST00000683680.1:c.94C>G ENSP00000507223.1:p.Arg32Gly
ENST00000684053.1:n.211C>G
ENST00000684163.1:c.85C>G ENSP00000508262.1:p.Arg29Gly
ENST00000684325.1:c.94C>G ENSP00000508121.1:p.Arg32Gly
ENST00000684385.1:c.94C>G ENSP00000507855.1:p.Arg32Gly
ENST00000684497.1:c.94C>G ENSP00000507057.1:p.Arg32Gly
ENST00000382292.9:c.94C>G MANE Select ENSP00000371729.3:p.Arg32Gly
ENST00000423156.2:c.94C>G ENSP00000390925.2:p.Arg32Gly
ENST00000455470.6:c.94C>G ENSP00000406565.2:p.Arg32Gly
ENST00000382292.7:c.94C>G ENSP00000371729.3:p.Arg32Gly
ENST00000382298.7:c.94C>G ENSP00000371735.3:p.Arg32Gly
ENST00000402364.1:c.-2069C>G ENSP00000385844.1:n.-2069C>G
NM_001278055.1:c.-260C>G NP_001264984.1:n.-260C>G
NM_014363.5:c.94C>G NP_055178.3:p.Arg32Gly
XM_005266338.1:c.94C>G XP_005266395.1:p.Arg32Gly
XM_011535038.1:c.118C>G XP_011533340.1:p.Arg40Gly
XM_011535039.1:c.85C>G XP_011533341.1:p.Arg29Gly
XM_005266338.2:c.94C>G XP_005266395.1:p.Arg32Gly
XM_011535039.2:c.85C>G XP_011533341.1:p.Arg29Gly
XM_017020539.1:c.85C>G XP_016876028.1:p.Arg29Gly
XM_024449337.1:c.94C>G XP_024305105.1:p.Arg32Gly
NM_014363.6:c.94C>G MANE Select NP_055178.3:p.Arg32Gly
NM_001278055.2:c.-260C>G NP_001264984.1:n.-260C>G