Canonical Allele Identifier: CA2078621974
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334790T= , CM000675.2:g.23334790T= GRCh38
NC_000013.10:g.23908929T= , CM000675.1:g.23908929T= GRCh37
NC_000013.9:g.22806929T= NCBI36
NG_012342.1:g.103913A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18995A= ENSP00000508399.1:n.2185+18995A=
ENST00000682944.1:c.9113A= ENSP00000507173.1:p.Asn3038=
ENST00000683210.1:c.2185+18995A= ENSP00000506739.1:n.2185+18995A=
ENST00000683270.1:c.6445+2632A= ENSP00000507624.1:n.6445+2632A=
ENST00000683367.1:c.2177-5306A= ENSP00000507780.1:n.2177-5306A=
ENST00000683489.1:c.2292-4838A= ENSP00000508403.1:n.2292-4838A=
ENST00000683680.1:c.2319-4838A= ENSP00000507223.1:n.2319-4838A=
ENST00000684163.1:c.2204-5306A= ENSP00000508262.1:n.2204-5306A=
ENST00000684196.1:n.4543-5306A=
ENST00000684325.1:c.2186-13116A= ENSP00000508121.1:n.2186-13116A=
ENST00000684385.1:c.2221-5306A= ENSP00000507855.1:n.2221-5306A=
ENST00000684497.1:c.2186-12146A= ENSP00000507057.1:n.2186-12146A=
ENST00000382292.9:c.9086A= MANE Select ENSP00000371729.3:p.Asn3029=
ENST00000423156.2:c.2186-5306A= ENSP00000390925.2:n.2186-5306A=
ENST00000455470.6:c.2432-5306A= ENSP00000406565.2:n.2432-5306A=
ENST00000382292.7:c.9086A= ENSP00000371729.3:p.Asn3029=
ENST00000382298.7:c.9086A= ENSP00000371735.3:p.Asn3029=
ENST00000402364.1:c.6836A= ENSP00000385844.1:p.Asn2279=
ENST00000423156.1:c.1058-5306A= ENSP00000390925.1:n.1058-5306A=
ENST00000455470.5:c.2130-5306A=
NM_001278055.1:c.8645A= NP_001264984.1:p.Asn2882=
NM_014363.5:c.9086A= NP_055178.3:p.Asn3029=
XM_005266338.1:c.9113A= XP_005266395.1:p.Asn3038=
XM_011535038.1:c.9137A= XP_011533340.1:p.Asn3046=
XM_011535039.1:c.9104A= XP_011533341.1:p.Asn3035=
XM_005266338.2:c.9113A= XP_005266395.1:p.Asn3038=
XM_011535039.2:c.9104A= XP_011533341.1:p.Asn3035=
XM_017020539.1:c.9077A= XP_016876028.1:p.Asn3026=
XM_024449337.1:c.9113A= XP_024305105.1:p.Asn3038=
NM_014363.6:c.9086A= MANE Select NP_055178.3:p.Asn3029=
NM_001278055.2:c.8645A= NP_001264984.1:p.Asn2882=