Canonical Allele Identifier: CA2078628328
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337948G= , CM000675.2:g.23337948G= GRCh38
NC_000013.10:g.23912087G= , CM000675.1:g.23912087G= GRCh37
NC_000013.9:g.22810087G= NCBI36
NG_012342.1:g.100755C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+15837C= ENSP00000508399.1:n.2185+15837C=
ENST00000682944.1:c.5955C= ENSP00000507173.1:p.Thr1985=
ENST00000683210.1:c.2185+15837C= ENSP00000506739.1:n.2185+15837C=
ENST00000683270.1:c.5919C= ENSP00000507624.1:p.Thr1973=
ENST00000683367.1:c.2177-8464C= ENSP00000507780.1:n.2177-8464C=
ENST00000683489.1:c.2291+3637C= ENSP00000508403.1:n.2291+3637C=
ENST00000683680.1:c.2318+3637C= ENSP00000507223.1:n.2318+3637C=
ENST00000684163.1:c.2204-8464C= ENSP00000508262.1:n.2204-8464C=
ENST00000684196.1:n.4543-8464C=
ENST00000684325.1:c.2185+15837C= ENSP00000508121.1:n.2185+15837C=
ENST00000684385.1:c.2221-8464C= ENSP00000507855.1:n.2221-8464C=
ENST00000684497.1:c.2186-15304C= ENSP00000507057.1:n.2186-15304C=
ENST00000382292.9:c.5928C= MANE Select ENSP00000371729.3:p.Thr1976=
ENST00000423156.2:c.2186-8464C= ENSP00000390925.2:n.2186-8464C=
ENST00000455470.6:c.2431+3497C= ENSP00000406565.2:n.2431+3497C=
ENST00000382292.7:c.5928C= ENSP00000371729.3:p.Thr1976=
ENST00000382298.7:c.5928C= ENSP00000371735.3:p.Thr1976=
ENST00000402364.1:c.3678C= ENSP00000385844.1:p.Thr1226=
ENST00000423156.1:c.1058-8464C= ENSP00000390925.1:n.1058-8464C=
ENST00000455470.5:c.2129+3497C=
NM_001278055.1:c.5487C= NP_001264984.1:p.Thr1829=
NM_014363.5:c.5928C= NP_055178.3:p.Thr1976=
XM_005266338.1:c.5955C= XP_005266395.1:p.Thr1985=
XM_011535038.1:c.5979C= XP_011533340.1:p.Thr1993=
XM_011535039.1:c.5946C= XP_011533341.1:p.Thr1982=
XM_005266338.2:c.5955C= XP_005266395.1:p.Thr1985=
XM_011535039.2:c.5946C= XP_011533341.1:p.Thr1982=
XM_017020539.1:c.5919C= XP_016876028.1:p.Thr1973=
XM_024449337.1:c.5955C= XP_024305105.1:p.Thr1985=
NM_014363.6:c.5928C= MANE Select NP_055178.3:p.Thr1976=
NM_001278055.2:c.5487C= NP_001264984.1:p.Thr1829=