Canonical Allele Identifier: CA6911855

Gene: SACS

Linked Data

• ClinVar Variation Id: 2884817
• ClinVar RCV Id: RCV003750466
• dbSNP Id: rs762515688
• ExAC: 13:23928991 G / C
• gnomAD v2: 13-23928991-G-C
• gnomAD v4: 13-23354852-G-C
• MyVariant Identifiers: chr13:g.23928991G>C (hg19) ; chr13:g.23354852G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23354852G>C , CM000675.2:g.23354852G>C	GRCh38
NC_000013.10:g.23928991G>C , CM000675.1:g.23928991G>C	GRCh37
NC_000013.9:g.22826991G>C	NCBI36
NG_012342.1:g.83851C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.1760C>G	ENSP00000508399.1:p.Thr587Arg
ENST00000682944.1:c.1760C>G	ENSP00000507173.1:p.Thr587Arg
ENST00000683154.1:n.1898C>G
ENST00000683210.1:c.1760C>G	ENSP00000506739.1:p.Thr587Arg
ENST00000683270.1:c.1751C>G	ENSP00000507624.1:p.Thr584Arg
ENST00000683367.1:c.1751C>G	ENSP00000507780.1:p.Thr584Arg
ENST00000683489.1:c.1760C>G	ENSP00000508403.1:p.Thr587Arg
ENST00000683680.1:c.1760C>G	ENSP00000507223.1:p.Thr587Arg
ENST00000684163.1:c.1751C>G	ENSP00000508262.1:p.Thr584Arg
ENST00000684196.1:n.4117C>G
ENST00000684325.1:c.1760C>G	ENSP00000508121.1:p.Thr587Arg
ENST00000684385.1:c.1760C>G	ENSP00000507855.1:p.Thr587Arg
ENST00000684497.1:c.1760C>G	ENSP00000507057.1:p.Thr587Arg
ENST00000382292.9:c.1760C>G MANE Select	ENSP00000371729.3:p.Thr587Arg
ENST00000423156.2:c.1760C>G	ENSP00000390925.2:p.Thr587Arg
ENST00000455470.6:c.1760C>G	ENSP00000406565.2:p.Thr587Arg
ENST00000382292.7:c.1760C>G	ENSP00000371729.3:p.Thr587Arg
ENST00000382298.7:c.1760C>G	ENSP00000371735.3:p.Thr587Arg
ENST00000402364.1:c.-491C>G	ENSP00000385844.1:n.-491C>G
ENST00000423156.1:c.632C>G	ENSP00000390925.1:p.Thr211Arg
ENST00000455470.5:c.1458C>G
ENST00000476776.1:n.39C>G
NM_001278055.1:c.1319C>G	NP_001264984.1:p.Thr440Arg
NM_014363.5:c.1760C>G	NP_055178.3:p.Thr587Arg
XM_005266338.1:c.1760C>G	XP_005266395.1:p.Thr587Arg
XM_011535038.1:c.1784C>G	XP_011533340.1:p.Thr595Arg
XM_011535039.1:c.1751C>G	XP_011533341.1:p.Thr584Arg
XM_005266338.2:c.1760C>G	XP_005266395.1:p.Thr587Arg
XM_011535039.2:c.1751C>G	XP_011533341.1:p.Thr584Arg
XM_017020539.1:c.1751C>G	XP_016876028.1:p.Thr584Arg
XM_024449337.1:c.1760C>G	XP_024305105.1:p.Thr587Arg
NM_014363.6:c.1760C>G MANE Select	NP_055178.3:p.Thr587Arg
NM_001278055.2:c.1319C>G	NP_001264984.1:p.Thr440Arg