Canonical Allele Identifier: CA6911196
Community Standard Title: NM_014363.6(SACS):c.5785C>T (p.Arg1929Trp)
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23338091G>A , CM000675.2:g.23338091G>A GRCh38
NC_000013.10:g.23912230G>A , CM000675.1:g.23912230G>A GRCh37
NC_000013.9:g.22810230G>A NCBI36
NG_012342.1:g.100612C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014363.6:c.5785C>T MANE Select NP_055178.3:p.Arg1929Trp
ENST00000382292.9:c.5785C>T MANE Select ENSP00000371729.3:p.Arg1929Trp
NM_001278055.1:c.5344C>T NP_001264984.1:p.Arg1782Trp
NM_001278055.2:c.5344C>T NP_001264984.1:p.Arg1782Trp
NM_014363.5:c.5785C>T NP_055178.3:p.Arg1929Trp
ENST00000382292.7:c.5785C>T ENSP00000371729.3:p.Arg1929Trp
ENST00000382298.7:c.5785C>T ENSP00000371735.3:p.Arg1929Trp
ENST00000402364.1:c.3535C>T ENSP00000385844.1:p.Arg1179Trp
ENST00000423156.1:c.1058-8607C>T ENSP00000390925.1:n.1058-8607C>T
ENST00000423156.2:c.2186-8607C>T ENSP00000390925.2:n.2186-8607C>T
ENST00000455470.5:c.2129+3354C>T
ENST00000455470.6:c.2431+3354C>T ENSP00000406565.2:n.2431+3354C>T
ENST00000682775.1:c.2185+15694C>T ENSP00000508399.1:n.2185+15694C>T
ENST00000682944.1:c.5812C>T ENSP00000507173.1:p.Arg1938Trp
ENST00000683210.1:c.2185+15694C>T ENSP00000506739.1:n.2185+15694C>T
ENST00000683270.1:c.5776C>T ENSP00000507624.1:p.Arg1926Trp
ENST00000683367.1:c.2177-8607C>T ENSP00000507780.1:n.2177-8607C>T
ENST00000683489.1:c.2291+3494C>T ENSP00000508403.1:n.2291+3494C>T
ENST00000683680.1:c.2318+3494C>T ENSP00000507223.1:n.2318+3494C>T
ENST00000684163.1:c.2204-8607C>T ENSP00000508262.1:n.2204-8607C>T
ENST00000684196.1:n.4543-8607C>T
ENST00000684325.1:c.2185+15694C>T ENSP00000508121.1:n.2185+15694C>T
ENST00000684385.1:c.2221-8607C>T ENSP00000507855.1:n.2221-8607C>T
ENST00000684497.1:c.2186-15447C>T ENSP00000507057.1:n.2186-15447C>T
XM_005266338.1:c.5812C>T XP_005266395.1:p.Arg1938Trp
XM_005266338.2:c.5812C>T XP_005266395.1:p.Arg1938Trp
XM_011535038.1:c.5836C>T XP_011533340.1:p.Arg1946Trp
XM_011535039.1:c.5803C>T XP_011533341.1:p.Arg1935Trp
XM_011535039.2:c.5803C>T XP_011533341.1:p.Arg1935Trp
XM_017020539.1:c.5776C>T XP_016876028.1:p.Arg1926Trp
XM_024449337.1:c.5812C>T XP_024305105.1:p.Arg1938Trp