Canonical Allele Identifier: CA6911507

Gene: SACS

Linked Data

• ClinVar Variation Id: 972058
• ClinVar RCV Id: RCV001247995 ; RCV001835319
• dbSNP Id: rs374961109
• ExAC: 13:23914464 G / C
• gnomAD v2: 13-23914464-G-C
• gnomAD v3: 13-23340325-G-C
• gnomAD v4: 13-23340325-G-C
• MyVariant Identifiers: chr13:g.23914464G>C (hg19) ; chr13:g.23340325G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23340325G>C , CM000675.2:g.23340325G>C	GRCh38
NC_000013.10:g.23914464G>C , CM000675.1:g.23914464G>C	GRCh37
NC_000013.9:g.22812464G>C	NCBI36
NG_012342.1:g.98378C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+13460C>G	ENSP00000508399.1:n.2185+13460C>G
ENST00000682944.1:c.3578C>G	ENSP00000507173.1:p.Pro1193Arg
ENST00000683210.1:c.2185+13460C>G	ENSP00000506739.1:n.2185+13460C>G
ENST00000683270.1:c.3542C>G	ENSP00000507624.1:p.Pro1181Arg
ENST00000683367.1:c.2177-10841C>G	ENSP00000507780.1:n.2177-10841C>G
ENST00000683489.1:c.2291+1260C>G	ENSP00000508403.1:n.2291+1260C>G
ENST00000683680.1:c.2318+1260C>G	ENSP00000507223.1:n.2318+1260C>G
ENST00000684163.1:c.2203+6486C>G	ENSP00000508262.1:n.2203+6486C>G
ENST00000684196.1:n.4543-10841C>G
ENST00000684325.1:c.2185+13460C>G	ENSP00000508121.1:n.2185+13460C>G
ENST00000684385.1:c.2220+6486C>G	ENSP00000507855.1:n.2220+6486C>G
ENST00000684497.1:c.2185+13460C>G	ENSP00000507057.1:n.2185+13460C>G
ENST00000382292.9:c.3551C>G MANE Select	ENSP00000371729.3:p.Pro1184Arg
ENST00000423156.2:c.2186-10841C>G	ENSP00000390925.2:n.2186-10841C>G
ENST00000455470.6:c.2431+1120C>G	ENSP00000406565.2:n.2431+1120C>G
ENST00000382292.7:c.3551C>G	ENSP00000371729.3:p.Pro1184Arg
ENST00000382298.7:c.3551C>G	ENSP00000371735.3:p.Pro1184Arg
ENST00000402364.1:c.1301C>G	ENSP00000385844.1:p.Pro434Arg
ENST00000423156.1:c.1058-10841C>G	ENSP00000390925.1:n.1058-10841C>G
ENST00000455470.5:c.2129+1120C>G
NM_001278055.1:c.3110C>G	NP_001264984.1:p.Pro1037Arg
NM_014363.5:c.3551C>G	NP_055178.3:p.Pro1184Arg
XM_005266338.1:c.3578C>G	XP_005266395.1:p.Pro1193Arg
XM_011535038.1:c.3602C>G	XP_011533340.1:p.Pro1201Arg
XM_011535039.1:c.3569C>G	XP_011533341.1:p.Pro1190Arg
XM_005266338.2:c.3578C>G	XP_005266395.1:p.Pro1193Arg
XM_011535039.2:c.3569C>G	XP_011533341.1:p.Pro1190Arg
XM_017020539.1:c.3542C>G	XP_016876028.1:p.Pro1181Arg
XM_024449337.1:c.3578C>G	XP_024305105.1:p.Pro1193Arg
NM_014363.6:c.3551C>G MANE Select	NP_055178.3:p.Pro1184Arg
NM_001278055.2:c.3110C>G	NP_001264984.1:p.Pro1037Arg