Canonical Allele Identifier: CA6911522
Gene: SACS HGNC NCBI

Linked Data

dbSNP Id: rs766188967

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23340450C>G , CM000675.2:g.23340450C>G GRCh38
NC_000013.10:g.23914589C>G , CM000675.1:g.23914589C>G GRCh37
NC_000013.9:g.22812589C>G NCBI36
NG_012342.1:g.98253G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+13335G>C ENSP00000508399.1:n.2185+13335G>C
ENST00000682944.1:c.3453G>C ENSP00000507173.1:p.Leu1151Phe
ENST00000683210.1:c.2185+13335G>C ENSP00000506739.1:n.2185+13335G>C
ENST00000683270.1:c.3417G>C ENSP00000507624.1:p.Leu1139Phe
ENST00000683367.1:c.2177-10966G>C ENSP00000507780.1:n.2177-10966G>C
ENST00000683489.1:c.2291+1135G>C ENSP00000508403.1:n.2291+1135G>C
ENST00000683680.1:c.2318+1135G>C ENSP00000507223.1:n.2318+1135G>C
ENST00000684163.1:c.2203+6361G>C ENSP00000508262.1:n.2203+6361G>C
ENST00000684196.1:n.4543-10966G>C
ENST00000684325.1:c.2185+13335G>C ENSP00000508121.1:n.2185+13335G>C
ENST00000684385.1:c.2220+6361G>C ENSP00000507855.1:n.2220+6361G>C
ENST00000684497.1:c.2185+13335G>C ENSP00000507057.1:n.2185+13335G>C
ENST00000382292.9:c.3426G>C MANE Select ENSP00000371729.3:p.Leu1142Phe
ENST00000423156.2:c.2186-10966G>C ENSP00000390925.2:n.2186-10966G>C
ENST00000455470.6:c.2431+995G>C ENSP00000406565.2:n.2431+995G>C
ENST00000382292.7:c.3426G>C ENSP00000371729.3:p.Leu1142Phe
ENST00000382298.7:c.3426G>C ENSP00000371735.3:p.Leu1142Phe
ENST00000402364.1:c.1176G>C ENSP00000385844.1:p.Leu392Phe
ENST00000423156.1:c.1058-10966G>C ENSP00000390925.1:n.1058-10966G>C
ENST00000455470.5:c.2129+995G>C
NM_001278055.1:c.2985G>C NP_001264984.1:p.Leu995Phe
NM_014363.5:c.3426G>C NP_055178.3:p.Leu1142Phe
XM_005266338.1:c.3453G>C XP_005266395.1:p.Leu1151Phe
XM_011535038.1:c.3477G>C XP_011533340.1:p.Leu1159Phe
XM_011535039.1:c.3444G>C XP_011533341.1:p.Leu1148Phe
XM_005266338.2:c.3453G>C XP_005266395.1:p.Leu1151Phe
XM_011535039.2:c.3444G>C XP_011533341.1:p.Leu1148Phe
XM_017020539.1:c.3417G>C XP_016876028.1:p.Leu1139Phe
XM_024449337.1:c.3453G>C XP_024305105.1:p.Leu1151Phe
NM_014363.6:c.3426G>C MANE Select NP_055178.3:p.Leu1142Phe
NM_001278055.2:c.2985G>C NP_001264984.1:p.Leu995Phe