Canonical Allele Identifier: CA2078646820
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23368257T= , CM000675.2:g.23368257T= GRCh38
NC_000013.10:g.23942396T= , CM000675.1:g.23942396T= GRCh37
NC_000013.9:g.22840396T= NCBI36
NG_012342.1:g.70446A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682244.1:n.918+145A=
ENST00000682354.1:n.1110+145A=
ENST00000682775.1:c.345+145A= ENSP00000508399.1:n.345+145A=
ENST00000682944.1:c.345+145A= ENSP00000507173.1:n.345+145A=
ENST00000683154.1:n.483+145A=
ENST00000683210.1:c.345+145A= ENSP00000506739.1:n.345+145A=
ENST00000683270.1:c.336+145A= ENSP00000507624.1:n.336+145A=
ENST00000683367.1:c.336+145A= ENSP00000507780.1:n.336+145A=
ENST00000683489.1:c.345+145A= ENSP00000508403.1:n.345+145A=
ENST00000683680.1:c.345+145A= ENSP00000507223.1:n.345+145A=
ENST00000684053.1:n.462+145A=
ENST00000684163.1:c.336+145A= ENSP00000508262.1:n.336+145A=
ENST00000684196.1:n.2702+145A=
ENST00000684325.1:c.345+145A= ENSP00000508121.1:n.345+145A=
ENST00000684385.1:c.345+145A= ENSP00000507855.1:n.345+145A=
ENST00000684497.1:c.345+145A= ENSP00000507057.1:n.345+145A=
ENST00000382292.9:c.345+145A= MANE Select ENSP00000371729.3:n.345+145A=
ENST00000423156.2:c.345+145A= ENSP00000390925.2:n.345+145A=
ENST00000455470.6:c.345+145A= ENSP00000406565.2:n.345+145A=
ENST00000382292.7:c.345+145A= ENSP00000371729.3:n.345+145A=
ENST00000382298.7:c.345+145A= ENSP00000371735.3:n.345+145A=
ENST00000402364.1:c.-1906+145A= ENSP00000385844.1:n.-1906+145A=
ENST00000455470.5:c.43+145A=
NM_001278055.1:c.-97+145A= NP_001264984.1:n.-97+145A=
NM_014363.5:c.345+145A= NP_055178.3:n.345+145A=
XM_005266338.1:c.345+145A= XP_005266395.1:n.345+145A=
XM_011535038.1:c.369+145A= XP_011533340.1:n.369+145A=
XM_011535039.1:c.336+145A= XP_011533341.1:n.336+145A=
XM_005266338.2:c.345+145A= XP_005266395.1:n.345+145A=
XM_011535039.2:c.336+145A= XP_011533341.1:n.336+145A=
XM_017020539.1:c.336+145A= XP_016876028.1:n.336+145A=
XM_024449337.1:c.345+145A= XP_024305105.1:n.345+145A=
NM_014363.6:c.345+145A= MANE Select NP_055178.3:n.345+145A=
NM_001278055.2:c.-97+145A= NP_001264984.1:n.-97+145A=