Canonical Allele Identifier: CA6910515

Gene: SACS

Linked Data

• ClinVar Variation Id: 311513
• ClinVar RCV Id: RCV000273799 ; RCV003750784
• dbSNP Id: rs372488932
• ExAC: 13:23907951 A / C
• gnomAD v2: 13-23907951-A-C
• gnomAD v4: 13-23333812-A-C
• MyVariant Identifiers: chr13:g.23907951A>C (hg19) ; chr13:g.23333812A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333812A>C , CM000675.2:g.23333812A>C	GRCh38
NC_000013.10:g.23907951A>C , CM000675.1:g.23907951A>C	GRCh37
NC_000013.9:g.22805951A>C	NCBI36
NG_012342.1:g.104891T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19973T>G	ENSP00000508399.1:n.2185+19973T>G
ENST00000682944.1:c.10091T>G	ENSP00000507173.1:p.Ile3364Arg
ENST00000683210.1:c.2185+19973T>G	ENSP00000506739.1:n.2185+19973T>G
ENST00000683270.1:c.6445+3610T>G	ENSP00000507624.1:n.6445+3610T>G
ENST00000683367.1:c.2177-4328T>G	ENSP00000507780.1:n.2177-4328T>G
ENST00000683489.1:c.2292-3860T>G	ENSP00000508403.1:n.2292-3860T>G
ENST00000683680.1:c.2319-3860T>G	ENSP00000507223.1:n.2319-3860T>G
ENST00000684163.1:c.2204-4328T>G	ENSP00000508262.1:n.2204-4328T>G
ENST00000684196.1:n.4543-4328T>G
ENST00000684325.1:c.2186-12138T>G	ENSP00000508121.1:n.2186-12138T>G
ENST00000684385.1:c.2221-4328T>G	ENSP00000507855.1:n.2221-4328T>G
ENST00000684497.1:c.2186-11168T>G	ENSP00000507057.1:n.2186-11168T>G
ENST00000382292.9:c.10064T>G MANE Select	ENSP00000371729.3:p.Ile3355Arg
ENST00000423156.2:c.2186-4328T>G	ENSP00000390925.2:n.2186-4328T>G
ENST00000455470.6:c.2432-4328T>G	ENSP00000406565.2:n.2432-4328T>G
ENST00000382292.7:c.10064T>G	ENSP00000371729.3:p.Ile3355Arg
ENST00000382298.7:c.10064T>G	ENSP00000371735.3:p.Ile3355Arg
ENST00000402364.1:c.7814T>G	ENSP00000385844.1:p.Ile2605Arg
ENST00000423156.1:c.1058-4328T>G	ENSP00000390925.1:n.1058-4328T>G
ENST00000455470.5:c.2130-4328T>G
NM_001278055.1:c.9623T>G	NP_001264984.1:p.Ile3208Arg
NM_014363.5:c.10064T>G	NP_055178.3:p.Ile3355Arg
XM_005266338.1:c.10091T>G	XP_005266395.1:p.Ile3364Arg
XM_011535038.1:c.10115T>G	XP_011533340.1:p.Ile3372Arg
XM_011535039.1:c.10082T>G	XP_011533341.1:p.Ile3361Arg
XM_005266338.2:c.10091T>G	XP_005266395.1:p.Ile3364Arg
XM_011535039.2:c.10082T>G	XP_011533341.1:p.Ile3361Arg
XM_017020539.1:c.10055T>G	XP_016876028.1:p.Ile3352Arg
XM_024449337.1:c.10091T>G	XP_024305105.1:p.Ile3364Arg
NM_014363.6:c.10064T>G MANE Select	NP_055178.3:p.Ile3355Arg
NM_001278055.2:c.9623T>G	NP_001264984.1:p.Ile3208Arg