Canonical Allele Identifier: CA483159925
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 766875
ClinVar RCV Id: RCV001424693
dbSNP Id: rs1373611853

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334996T>C , CM000675.2:g.23334996T>C GRCh38
NC_000013.10:g.23909135T>C , CM000675.1:g.23909135T>C GRCh37
NC_000013.9:g.22807135T>C NCBI36
NG_012342.1:g.103707A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+18789A>G ENSP00000508399.1:n.2185+18789A>G
ENST00000682944.1:c.8907A>G ENSP00000507173.1:p.Leu2969=
ENST00000683210.1:c.2185+18789A>G ENSP00000506739.1:n.2185+18789A>G
ENST00000683270.1:c.6445+2426A>G ENSP00000507624.1:n.6445+2426A>G
ENST00000683367.1:c.2177-5512A>G ENSP00000507780.1:n.2177-5512A>G
ENST00000683489.1:c.2292-5044A>G ENSP00000508403.1:n.2292-5044A>G
ENST00000683680.1:c.2319-5044A>G ENSP00000507223.1:n.2319-5044A>G
ENST00000684163.1:c.2204-5512A>G ENSP00000508262.1:n.2204-5512A>G
ENST00000684196.1:n.4543-5512A>G
ENST00000684325.1:c.2186-13322A>G ENSP00000508121.1:n.2186-13322A>G
ENST00000684385.1:c.2221-5512A>G ENSP00000507855.1:n.2221-5512A>G
ENST00000684497.1:c.2186-12352A>G ENSP00000507057.1:n.2186-12352A>G
ENST00000382292.9:c.8880A>G MANE Select ENSP00000371729.3:p.Leu2960=
ENST00000423156.2:c.2186-5512A>G ENSP00000390925.2:n.2186-5512A>G
ENST00000455470.6:c.2432-5512A>G ENSP00000406565.2:n.2432-5512A>G
ENST00000382292.7:c.8880A>G ENSP00000371729.3:p.Leu2960=
ENST00000382298.7:c.8880A>G ENSP00000371735.3:p.Leu2960=
ENST00000402364.1:c.6630A>G ENSP00000385844.1:p.Leu2210=
ENST00000423156.1:c.1058-5512A>G ENSP00000390925.1:n.1058-5512A>G
ENST00000455470.5:c.2130-5512A>G
NM_001278055.1:c.8439A>G NP_001264984.1:p.Leu2813=
NM_014363.5:c.8880A>G NP_055178.3:p.Leu2960=
XM_005266338.1:c.8907A>G XP_005266395.1:p.Leu2969=
XM_011535038.1:c.8931A>G XP_011533340.1:p.Leu2977=
XM_011535039.1:c.8898A>G XP_011533341.1:p.Leu2966=
XM_005266338.2:c.8907A>G XP_005266395.1:p.Leu2969=
XM_011535039.2:c.8898A>G XP_011533341.1:p.Leu2966=
XM_017020539.1:c.8871A>G XP_016876028.1:p.Leu2957=
XM_024449337.1:c.8907A>G XP_024305105.1:p.Leu2969=
NM_014363.6:c.8880A>G MANE Select NP_055178.3:p.Leu2960=
NM_001278055.2:c.8439A>G NP_001264984.1:p.Leu2813=