Canonical Allele Identifier: CA6911170
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311538
dbSNP Id: rs774492331

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23337946T>C , CM000675.2:g.23337946T>C GRCh38
NC_000013.10:g.23912085T>C , CM000675.1:g.23912085T>C GRCh37
NC_000013.9:g.22810085T>C NCBI36
NG_012342.1:g.100757A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+15839A>G ENSP00000508399.1:n.2185+15839A>G
ENST00000682944.1:c.5957A>G ENSP00000507173.1:p.Lys1986Arg
ENST00000683210.1:c.2185+15839A>G ENSP00000506739.1:n.2185+15839A>G
ENST00000683270.1:c.5921A>G ENSP00000507624.1:p.Lys1974Arg
ENST00000683367.1:c.2177-8462A>G ENSP00000507780.1:n.2177-8462A>G
ENST00000683489.1:c.2291+3639A>G ENSP00000508403.1:n.2291+3639A>G
ENST00000683680.1:c.2318+3639A>G ENSP00000507223.1:n.2318+3639A>G
ENST00000684163.1:c.2204-8462A>G ENSP00000508262.1:n.2204-8462A>G
ENST00000684196.1:n.4543-8462A>G
ENST00000684325.1:c.2185+15839A>G ENSP00000508121.1:n.2185+15839A>G
ENST00000684385.1:c.2221-8462A>G ENSP00000507855.1:n.2221-8462A>G
ENST00000684497.1:c.2186-15302A>G ENSP00000507057.1:n.2186-15302A>G
ENST00000382292.9:c.5930A>G MANE Select ENSP00000371729.3:p.Lys1977Arg
ENST00000423156.2:c.2186-8462A>G ENSP00000390925.2:n.2186-8462A>G
ENST00000455470.6:c.2431+3499A>G ENSP00000406565.2:n.2431+3499A>G
ENST00000382292.7:c.5930A>G ENSP00000371729.3:p.Lys1977Arg
ENST00000382298.7:c.5930A>G ENSP00000371735.3:p.Lys1977Arg
ENST00000402364.1:c.3680A>G ENSP00000385844.1:p.Lys1227Arg
ENST00000423156.1:c.1058-8462A>G ENSP00000390925.1:n.1058-8462A>G
ENST00000455470.5:c.2129+3499A>G
NM_001278055.1:c.5489A>G NP_001264984.1:p.Lys1830Arg
NM_014363.5:c.5930A>G NP_055178.3:p.Lys1977Arg
XM_005266338.1:c.5957A>G XP_005266395.1:p.Lys1986Arg
XM_011535038.1:c.5981A>G XP_011533340.1:p.Lys1994Arg
XM_011535039.1:c.5948A>G XP_011533341.1:p.Lys1983Arg
XM_005266338.2:c.5957A>G XP_005266395.1:p.Lys1986Arg
XM_011535039.2:c.5948A>G XP_011533341.1:p.Lys1983Arg
XM_017020539.1:c.5921A>G XP_016876028.1:p.Lys1974Arg
XM_024449337.1:c.5957A>G XP_024305105.1:p.Lys1986Arg
NM_014363.6:c.5930A>G MANE Select NP_055178.3:p.Lys1977Arg
NM_001278055.2:c.5489A>G NP_001264984.1:p.Lys1830Arg