Canonical Allele Identifier: CA6910386
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 990735
ClinVar RCV Id: RCV001278819
dbSNP Id: rs372494676

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333057T>C , CM000675.2:g.23333057T>C GRCh38
NC_000013.10:g.23907196T>C , CM000675.1:g.23907196T>C GRCh37
NC_000013.9:g.22805196T>C NCBI36
NG_012342.1:g.105646A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+20728A>G ENSP00000508399.1:n.2185+20728A>G
ENST00000682944.1:c.10846A>G ENSP00000507173.1:p.Ile3616Val
ENST00000683210.1:c.2185+20728A>G ENSP00000506739.1:n.2185+20728A>G
ENST00000683270.1:c.6446-3573A>G ENSP00000507624.1:n.6446-3573A>G
ENST00000683367.1:c.2177-3573A>G ENSP00000507780.1:n.2177-3573A>G
ENST00000683489.1:c.2292-3105A>G ENSP00000508403.1:n.2292-3105A>G
ENST00000683680.1:c.2319-3105A>G ENSP00000507223.1:n.2319-3105A>G
ENST00000684163.1:c.2204-3573A>G ENSP00000508262.1:n.2204-3573A>G
ENST00000684196.1:n.4543-3573A>G
ENST00000684325.1:c.2186-11383A>G ENSP00000508121.1:n.2186-11383A>G
ENST00000684385.1:c.2221-3573A>G ENSP00000507855.1:n.2221-3573A>G
ENST00000684497.1:c.2186-10413A>G ENSP00000507057.1:n.2186-10413A>G
ENST00000382292.9:c.10819A>G MANE Select ENSP00000371729.3:p.Ile3607Val
ENST00000423156.2:c.2186-3573A>G ENSP00000390925.2:n.2186-3573A>G
ENST00000455470.6:c.2432-3573A>G ENSP00000406565.2:n.2432-3573A>G
ENST00000382292.7:c.10819A>G ENSP00000371729.3:p.Ile3607Val
ENST00000382298.7:c.10819A>G ENSP00000371735.3:p.Ile3607Val
ENST00000402364.1:c.8569A>G ENSP00000385844.1:p.Ile2857Val
ENST00000423156.1:c.1058-3573A>G ENSP00000390925.1:n.1058-3573A>G
ENST00000455470.5:c.2130-3573A>G
NM_001278055.1:c.10378A>G NP_001264984.1:p.Ile3460Val
NM_014363.5:c.10819A>G NP_055178.3:p.Ile3607Val
XM_005266338.1:c.10846A>G XP_005266395.1:p.Ile3616Val
XM_011535038.1:c.10870A>G XP_011533340.1:p.Ile3624Val
XM_011535039.1:c.10837A>G XP_011533341.1:p.Ile3613Val
XM_005266338.2:c.10846A>G XP_005266395.1:p.Ile3616Val
XM_011535039.2:c.10837A>G XP_011533341.1:p.Ile3613Val
XM_017020539.1:c.10810A>G XP_016876028.1:p.Ile3604Val
XM_024449337.1:c.10846A>G XP_024305105.1:p.Ile3616Val
NM_014363.6:c.10819A>G MANE Select NP_055178.3:p.Ile3607Val
NM_001278055.2:c.10378A>G NP_001264984.1:p.Ile3460Val