Canonical Allele Identifier: CA2078622943
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23335259G= , CM000675.2:g.23335259G= GRCh38
NC_000013.10:g.23909398G= , CM000675.1:g.23909398G= GRCh37
NC_000013.9:g.22807398G= NCBI36
NG_012342.1:g.103444C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18526C= ENSP00000508399.1:n.2185+18526C=
ENST00000682944.1:c.8644C= ENSP00000507173.1:p.Leu2882=
ENST00000683210.1:c.2185+18526C= ENSP00000506739.1:n.2185+18526C=
ENST00000683270.1:c.6445+2163C= ENSP00000507624.1:n.6445+2163C=
ENST00000683367.1:c.2177-5775C= ENSP00000507780.1:n.2177-5775C=
ENST00000683489.1:c.2292-5307C= ENSP00000508403.1:n.2292-5307C=
ENST00000683680.1:c.2319-5307C= ENSP00000507223.1:n.2319-5307C=
ENST00000684163.1:c.2204-5775C= ENSP00000508262.1:n.2204-5775C=
ENST00000684196.1:n.4543-5775C=
ENST00000684325.1:c.2186-13585C= ENSP00000508121.1:n.2186-13585C=
ENST00000684385.1:c.2221-5775C= ENSP00000507855.1:n.2221-5775C=
ENST00000684497.1:c.2186-12615C= ENSP00000507057.1:n.2186-12615C=
ENST00000382292.9:c.8617C= MANE Select ENSP00000371729.3:p.Leu2873=
ENST00000423156.2:c.2186-5775C= ENSP00000390925.2:n.2186-5775C=
ENST00000455470.6:c.2432-5775C= ENSP00000406565.2:n.2432-5775C=
ENST00000382292.7:c.8617C= ENSP00000371729.3:p.Leu2873=
ENST00000382298.7:c.8617C= ENSP00000371735.3:p.Leu2873=
ENST00000402364.1:c.6367C= ENSP00000385844.1:p.Leu2123=
ENST00000423156.1:c.1058-5775C= ENSP00000390925.1:n.1058-5775C=
ENST00000455470.5:c.2130-5775C=
NM_001278055.1:c.8176C= NP_001264984.1:p.Leu2726=
NM_014363.5:c.8617C= NP_055178.3:p.Leu2873=
XM_005266338.1:c.8644C= XP_005266395.1:p.Leu2882=
XM_011535038.1:c.8668C= XP_011533340.1:p.Leu2890=
XM_011535039.1:c.8635C= XP_011533341.1:p.Leu2879=
XM_005266338.2:c.8644C= XP_005266395.1:p.Leu2882=
XM_011535039.2:c.8635C= XP_011533341.1:p.Leu2879=
XM_017020539.1:c.8608C= XP_016876028.1:p.Leu2870=
XM_024449337.1:c.8644C= XP_024305105.1:p.Leu2882=
NM_014363.6:c.8617C= MANE Select NP_055178.3:p.Leu2873=
NM_001278055.2:c.8176C= NP_001264984.1:p.Leu2726=