Canonical Allele Identifier: CA2078641131
Community Standard Title: NM_014363.6(SACS):c.4095G= (p.Trp1365=)
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23339781C= , CM000675.2:g.23339781C= GRCh38
NC_000013.10:g.23913920C= , CM000675.1:g.23913920C= GRCh37
NC_000013.9:g.22811920C= NCBI36
NG_012342.1:g.98922G=

Transcript Alleles

HGVS Amino-acid Change
NM_014363.6:c.4095G= MANE Select NP_055178.3:p.Trp1365=
ENST00000382292.9:c.4095G= MANE Select ENSP00000371729.3:p.Trp1365=
NM_001278055.1:c.3654G= NP_001264984.1:p.Trp1218=
NM_001278055.2:c.3654G= NP_001264984.1:p.Trp1218=
NM_014363.5:c.4095G= NP_055178.3:p.Trp1365=
ENST00000382292.7:c.4095G= ENSP00000371729.3:p.Trp1365=
ENST00000382298.7:c.4095G= ENSP00000371735.3:p.Trp1365=
ENST00000402364.1:c.1845G= ENSP00000385844.1:p.Trp615=
ENST00000423156.1:c.1058-10297G= ENSP00000390925.1:n.1058-10297G=
ENST00000423156.2:c.2186-10297G= ENSP00000390925.2:n.2186-10297G=
ENST00000455470.5:c.2129+1664G=
ENST00000455470.6:c.2431+1664G= ENSP00000406565.2:n.2431+1664G=
ENST00000682775.1:c.2185+14004G= ENSP00000508399.1:n.2185+14004G=
ENST00000682944.1:c.4122G= ENSP00000507173.1:p.Trp1374=
ENST00000683210.1:c.2185+14004G= ENSP00000506739.1:n.2185+14004G=
ENST00000683270.1:c.4086G= ENSP00000507624.1:p.Trp1362=
ENST00000683367.1:c.2177-10297G= ENSP00000507780.1:n.2177-10297G=
ENST00000683489.1:c.2291+1804G= ENSP00000508403.1:n.2291+1804G=
ENST00000683680.1:c.2318+1804G= ENSP00000507223.1:n.2318+1804G=
ENST00000684163.1:c.2203+7030G= ENSP00000508262.1:n.2203+7030G=
ENST00000684196.1:n.4543-10297G=
ENST00000684325.1:c.2185+14004G= ENSP00000508121.1:n.2185+14004G=
ENST00000684385.1:c.2220+7030G= ENSP00000507855.1:n.2220+7030G=
ENST00000684497.1:c.2185+14004G= ENSP00000507057.1:n.2185+14004G=
XM_005266338.1:c.4122G= XP_005266395.1:p.Trp1374=
XM_005266338.2:c.4122G= XP_005266395.1:p.Trp1374=
XM_011535038.1:c.4146G= XP_011533340.1:p.Trp1382=
XM_011535039.1:c.4113G= XP_011533341.1:p.Trp1371=
XM_011535039.2:c.4113G= XP_011533341.1:p.Trp1371=
XM_017020539.1:c.4086G= XP_016876028.1:p.Trp1362=
XM_024449337.1:c.4122G= XP_024305105.1:p.Trp1374=