Canonical Allele Identifier: CA387527941
Community Standard Title: NM_014363.6(SACS):c.4723C>T (p.Arg1575Trp)
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23339153G>A , CM000675.2:g.23339153G>A GRCh38
NC_000013.10:g.23913292G>A , CM000675.1:g.23913292G>A GRCh37
NC_000013.9:g.22811292G>A NCBI36
NG_012342.1:g.99550C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014363.6:c.4723C>T MANE Select NP_055178.3:p.Arg1575Trp
ENST00000382292.9:c.4723C>T MANE Select ENSP00000371729.3:p.Arg1575Trp
NM_001278055.1:c.4282C>T NP_001264984.1:p.Arg1428Trp
NM_001278055.2:c.4282C>T NP_001264984.1:p.Arg1428Trp
NM_014363.5:c.4723C>T NP_055178.3:p.Arg1575Trp
ENST00000382292.7:c.4723C>T ENSP00000371729.3:p.Arg1575Trp
ENST00000382298.7:c.4723C>T ENSP00000371735.3:p.Arg1575Trp
ENST00000402364.1:c.2473C>T ENSP00000385844.1:p.Arg825Trp
ENST00000423156.1:c.1058-9669C>T ENSP00000390925.1:n.1058-9669C>T
ENST00000423156.2:c.2186-9669C>T ENSP00000390925.2:n.2186-9669C>T
ENST00000455470.5:c.2129+2292C>T
ENST00000455470.6:c.2431+2292C>T ENSP00000406565.2:n.2431+2292C>T
ENST00000682775.1:c.2185+14632C>T ENSP00000508399.1:n.2185+14632C>T
ENST00000682944.1:c.4750C>T ENSP00000507173.1:p.Arg1584Trp
ENST00000683210.1:c.2185+14632C>T ENSP00000506739.1:n.2185+14632C>T
ENST00000683270.1:c.4714C>T ENSP00000507624.1:p.Arg1572Trp
ENST00000683367.1:c.2177-9669C>T ENSP00000507780.1:n.2177-9669C>T
ENST00000683489.1:c.2291+2432C>T ENSP00000508403.1:n.2291+2432C>T
ENST00000683680.1:c.2318+2432C>T ENSP00000507223.1:n.2318+2432C>T
ENST00000684163.1:c.2203+7658C>T ENSP00000508262.1:n.2203+7658C>T
ENST00000684196.1:n.4543-9669C>T
ENST00000684325.1:c.2185+14632C>T ENSP00000508121.1:n.2185+14632C>T
ENST00000684385.1:c.2220+7658C>T ENSP00000507855.1:n.2220+7658C>T
ENST00000684497.1:c.2185+14632C>T ENSP00000507057.1:n.2185+14632C>T
XM_005266338.1:c.4750C>T XP_005266395.1:p.Arg1584Trp
XM_005266338.2:c.4750C>T XP_005266395.1:p.Arg1584Trp
XM_011535038.1:c.4774C>T XP_011533340.1:p.Arg1592Trp
XM_011535039.1:c.4741C>T XP_011533341.1:p.Arg1581Trp
XM_011535039.2:c.4741C>T XP_011533341.1:p.Arg1581Trp
XM_017020539.1:c.4714C>T XP_016876028.1:p.Arg1572Trp
XM_024449337.1:c.4750C>T XP_024305105.1:p.Arg1584Trp