Canonical Allele Identifier: CA387549321
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23355333A>G , CM000675.2:g.23355333A>G GRCh38
NC_000013.10:g.23929472A>G , CM000675.1:g.23929472A>G GRCh37
NC_000013.9:g.22827472A>G NCBI36
NG_012342.1:g.83370T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.1279T>C ENSP00000508399.1:p.Ser427Pro
ENST00000682944.1:c.1279T>C ENSP00000507173.1:p.Ser427Pro
ENST00000683154.1:n.1417T>C
ENST00000683210.1:c.1279T>C ENSP00000506739.1:p.Ser427Pro
ENST00000683270.1:c.1270T>C ENSP00000507624.1:p.Ser424Pro
ENST00000683367.1:c.1270T>C ENSP00000507780.1:p.Ser424Pro
ENST00000683489.1:c.1279T>C ENSP00000508403.1:p.Ser427Pro
ENST00000683680.1:c.1279T>C ENSP00000507223.1:p.Ser427Pro
ENST00000684163.1:c.1270T>C ENSP00000508262.1:p.Ser424Pro
ENST00000684196.1:n.3636T>C
ENST00000684325.1:c.1279T>C ENSP00000508121.1:p.Ser427Pro
ENST00000684385.1:c.1279T>C ENSP00000507855.1:p.Ser427Pro
ENST00000684497.1:c.1279T>C ENSP00000507057.1:p.Ser427Pro
ENST00000382292.9:c.1279T>C MANE Select ENSP00000371729.3:p.Ser427Pro
ENST00000423156.2:c.1279T>C ENSP00000390925.2:p.Ser427Pro
ENST00000455470.6:c.1279T>C ENSP00000406565.2:p.Ser427Pro
ENST00000382292.7:c.1279T>C ENSP00000371729.3:p.Ser427Pro
ENST00000382298.7:c.1279T>C ENSP00000371735.3:p.Ser427Pro
ENST00000402364.1:c.-972T>C ENSP00000385844.1:n.-972T>C
ENST00000423156.1:c.151T>C ENSP00000390925.1:p.Ser51Pro
ENST00000455470.5:c.977T>C
NM_001278055.1:c.838T>C NP_001264984.1:p.Ser280Pro
NM_014363.5:c.1279T>C NP_055178.3:p.Ser427Pro
XM_005266338.1:c.1279T>C XP_005266395.1:p.Ser427Pro
XM_011535038.1:c.1303T>C XP_011533340.1:p.Ser435Pro
XM_011535039.1:c.1270T>C XP_011533341.1:p.Ser424Pro
XM_005266338.2:c.1279T>C XP_005266395.1:p.Ser427Pro
XM_011535039.2:c.1270T>C XP_011533341.1:p.Ser424Pro
XM_017020539.1:c.1270T>C XP_016876028.1:p.Ser424Pro
XM_024449337.1:c.1279T>C XP_024305105.1:p.Ser427Pro
NM_014363.6:c.1279T>C MANE Select NP_055178.3:p.Ser427Pro
NM_001278055.2:c.838T>C NP_001264984.1:p.Ser280Pro