Canonical Allele Identifier: CA2078628157
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337868T= , CM000675.2:g.23337868T= GRCh38
NC_000013.10:g.23912007T= , CM000675.1:g.23912007T= GRCh37
NC_000013.9:g.22810007T= NCBI36
NG_012342.1:g.100835A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+15917A= ENSP00000508399.1:n.2185+15917A=
ENST00000682944.1:c.6035A= ENSP00000507173.1:p.Asp2012=
ENST00000683210.1:c.2185+15917A= ENSP00000506739.1:n.2185+15917A=
ENST00000683270.1:c.5999A= ENSP00000507624.1:p.Asp2000=
ENST00000683367.1:c.2177-8384A= ENSP00000507780.1:n.2177-8384A=
ENST00000683489.1:c.2291+3717A= ENSP00000508403.1:n.2291+3717A=
ENST00000683680.1:c.2318+3717A= ENSP00000507223.1:n.2318+3717A=
ENST00000684163.1:c.2204-8384A= ENSP00000508262.1:n.2204-8384A=
ENST00000684196.1:n.4543-8384A=
ENST00000684325.1:c.2185+15917A= ENSP00000508121.1:n.2185+15917A=
ENST00000684385.1:c.2221-8384A= ENSP00000507855.1:n.2221-8384A=
ENST00000684497.1:c.2186-15224A= ENSP00000507057.1:n.2186-15224A=
ENST00000382292.9:c.6008A= MANE Select ENSP00000371729.3:p.Asp2003=
ENST00000423156.2:c.2186-8384A= ENSP00000390925.2:n.2186-8384A=
ENST00000455470.6:c.2431+3577A= ENSP00000406565.2:n.2431+3577A=
ENST00000382292.7:c.6008A= ENSP00000371729.3:p.Asp2003=
ENST00000382298.7:c.6008A= ENSP00000371735.3:p.Asp2003=
ENST00000402364.1:c.3758A= ENSP00000385844.1:p.Asp1253=
ENST00000423156.1:c.1058-8384A= ENSP00000390925.1:n.1058-8384A=
ENST00000455470.5:c.2129+3577A=
NM_001278055.1:c.5567A= NP_001264984.1:p.Asp1856=
NM_014363.5:c.6008A= NP_055178.3:p.Asp2003=
XM_005266338.1:c.6035A= XP_005266395.1:p.Asp2012=
XM_011535038.1:c.6059A= XP_011533340.1:p.Asp2020=
XM_011535039.1:c.6026A= XP_011533341.1:p.Asp2009=
XM_005266338.2:c.6035A= XP_005266395.1:p.Asp2012=
XM_011535039.2:c.6026A= XP_011533341.1:p.Asp2009=
XM_017020539.1:c.5999A= XP_016876028.1:p.Asp2000=
XM_024449337.1:c.6035A= XP_024305105.1:p.Asp2012=
NM_014363.6:c.6008A= MANE Select NP_055178.3:p.Asp2003=
NM_001278055.2:c.5567A= NP_001264984.1:p.Asp1856=