Canonical Allele Identifier: CA387524268
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337947T>A , CM000675.2:g.23337947T>A GRCh38
NC_000013.10:g.23912086T>A , CM000675.1:g.23912086T>A GRCh37
NC_000013.9:g.22810086T>A NCBI36
NG_012342.1:g.100756A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+15838A>T ENSP00000508399.1:n.2185+15838A>T
ENST00000682944.1:c.5956A>T ENSP00000507173.1:p.Lys1986Ter
ENST00000683210.1:c.2185+15838A>T ENSP00000506739.1:n.2185+15838A>T
ENST00000683270.1:c.5920A>T ENSP00000507624.1:p.Lys1974Ter
ENST00000683367.1:c.2177-8463A>T ENSP00000507780.1:n.2177-8463A>T
ENST00000683489.1:c.2291+3638A>T ENSP00000508403.1:n.2291+3638A>T
ENST00000683680.1:c.2318+3638A>T ENSP00000507223.1:n.2318+3638A>T
ENST00000684163.1:c.2204-8463A>T ENSP00000508262.1:n.2204-8463A>T
ENST00000684196.1:n.4543-8463A>T
ENST00000684325.1:c.2185+15838A>T ENSP00000508121.1:n.2185+15838A>T
ENST00000684385.1:c.2221-8463A>T ENSP00000507855.1:n.2221-8463A>T
ENST00000684497.1:c.2186-15303A>T ENSP00000507057.1:n.2186-15303A>T
ENST00000382292.9:c.5929A>T MANE Select ENSP00000371729.3:p.Lys1977Ter
ENST00000423156.2:c.2186-8463A>T ENSP00000390925.2:n.2186-8463A>T
ENST00000455470.6:c.2431+3498A>T ENSP00000406565.2:n.2431+3498A>T
ENST00000382292.7:c.5929A>T ENSP00000371729.3:p.Lys1977Ter
ENST00000382298.7:c.5929A>T ENSP00000371735.3:p.Lys1977Ter
ENST00000402364.1:c.3679A>T ENSP00000385844.1:p.Lys1227Ter
ENST00000423156.1:c.1058-8463A>T ENSP00000390925.1:n.1058-8463A>T
ENST00000455470.5:c.2129+3498A>T
NM_001278055.1:c.5488A>T NP_001264984.1:p.Lys1830Ter
NM_014363.5:c.5929A>T NP_055178.3:p.Lys1977Ter
XM_005266338.1:c.5956A>T XP_005266395.1:p.Lys1986Ter
XM_011535038.1:c.5980A>T XP_011533340.1:p.Lys1994Ter
XM_011535039.1:c.5947A>T XP_011533341.1:p.Lys1983Ter
XM_005266338.2:c.5956A>T XP_005266395.1:p.Lys1986Ter
XM_011535039.2:c.5947A>T XP_011533341.1:p.Lys1983Ter
XM_017020539.1:c.5920A>T XP_016876028.1:p.Lys1974Ter
XM_024449337.1:c.5956A>T XP_024305105.1:p.Lys1986Ter
NM_014363.6:c.5929A>T MANE Select NP_055178.3:p.Lys1977Ter
NM_001278055.2:c.5488A>T NP_001264984.1:p.Lys1830Ter