Canonical Allele Identifier: CA2078621726
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334655T= , CM000675.2:g.23334655T= GRCh38
NC_000013.10:g.23908794T= , CM000675.1:g.23908794T= GRCh37
NC_000013.9:g.22806794T= NCBI36
NG_012342.1:g.104048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+19130A= ENSP00000508399.1:n.2185+19130A=
ENST00000682944.1:c.9248A= ENSP00000507173.1:p.Asp3083=
ENST00000683210.1:c.2185+19130A= ENSP00000506739.1:n.2185+19130A=
ENST00000683270.1:c.6445+2767A= ENSP00000507624.1:n.6445+2767A=
ENST00000683367.1:c.2177-5171A= ENSP00000507780.1:n.2177-5171A=
ENST00000683489.1:c.2292-4703A= ENSP00000508403.1:n.2292-4703A=
ENST00000683680.1:c.2319-4703A= ENSP00000507223.1:n.2319-4703A=
ENST00000684163.1:c.2204-5171A= ENSP00000508262.1:n.2204-5171A=
ENST00000684196.1:n.4543-5171A=
ENST00000684325.1:c.2186-12981A= ENSP00000508121.1:n.2186-12981A=
ENST00000684385.1:c.2221-5171A= ENSP00000507855.1:n.2221-5171A=
ENST00000684497.1:c.2186-12011A= ENSP00000507057.1:n.2186-12011A=
ENST00000382292.9:c.9221A= MANE Select ENSP00000371729.3:p.Asp3074=
ENST00000423156.2:c.2186-5171A= ENSP00000390925.2:n.2186-5171A=
ENST00000455470.6:c.2432-5171A= ENSP00000406565.2:n.2432-5171A=
ENST00000382292.7:c.9221A= ENSP00000371729.3:p.Asp3074=
ENST00000382298.7:c.9221A= ENSP00000371735.3:p.Asp3074=
ENST00000402364.1:c.6971A= ENSP00000385844.1:p.Asp2324=
ENST00000423156.1:c.1058-5171A= ENSP00000390925.1:n.1058-5171A=
ENST00000455470.5:c.2130-5171A=
NM_001278055.1:c.8780A= NP_001264984.1:p.Asp2927=
NM_014363.5:c.9221A= NP_055178.3:p.Asp3074=
XM_005266338.1:c.9248A= XP_005266395.1:p.Asp3083=
XM_011535038.1:c.9272A= XP_011533340.1:p.Asp3091=
XM_011535039.1:c.9239A= XP_011533341.1:p.Asp3080=
XM_005266338.2:c.9248A= XP_005266395.1:p.Asp3083=
XM_011535039.2:c.9239A= XP_011533341.1:p.Asp3080=
XM_017020539.1:c.9212A= XP_016876028.1:p.Asp3071=
XM_024449337.1:c.9248A= XP_024305105.1:p.Asp3083=
NM_014363.6:c.9221A= MANE Select NP_055178.3:p.Asp3074=
NM_001278055.2:c.8780A= NP_001264984.1:p.Asp2927=