Canonical Allele Identifier: CA6910611

Gene: SACS

Linked Data

• ClinVar Variation Id: 1122598
• ClinVar RCV Id: RCV001453295 ; RCV003399241
• dbSNP Id: rs369043814
• ExAC: 13:23908490 T / C
• gnomAD v2: 13-23908490-T-C
• gnomAD v3: 13-23334351-T-C
• gnomAD v4: 13-23334351-T-C
• MyVariant Identifiers: chr13:g.23908490T>C (hg19) ; chr13:g.23334351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334351T>C , CM000675.2:g.23334351T>C	GRCh38
NC_000013.10:g.23908490T>C , CM000675.1:g.23908490T>C	GRCh37
NC_000013.9:g.22806490T>C	NCBI36
NG_012342.1:g.104352A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19434A>G	ENSP00000508399.1:n.2185+19434A>G
ENST00000682944.1:c.9552A>G	ENSP00000507173.1:p.Thr3184=
ENST00000683210.1:c.2185+19434A>G	ENSP00000506739.1:n.2185+19434A>G
ENST00000683270.1:c.6445+3071A>G	ENSP00000507624.1:n.6445+3071A>G
ENST00000683367.1:c.2177-4867A>G	ENSP00000507780.1:n.2177-4867A>G
ENST00000683489.1:c.2292-4399A>G	ENSP00000508403.1:n.2292-4399A>G
ENST00000683680.1:c.2319-4399A>G	ENSP00000507223.1:n.2319-4399A>G
ENST00000684163.1:c.2204-4867A>G	ENSP00000508262.1:n.2204-4867A>G
ENST00000684196.1:n.4543-4867A>G
ENST00000684325.1:c.2186-12677A>G	ENSP00000508121.1:n.2186-12677A>G
ENST00000684385.1:c.2221-4867A>G	ENSP00000507855.1:n.2221-4867A>G
ENST00000684497.1:c.2186-11707A>G	ENSP00000507057.1:n.2186-11707A>G
ENST00000382292.9:c.9525A>G MANE Select	ENSP00000371729.3:p.Thr3175=
ENST00000423156.2:c.2186-4867A>G	ENSP00000390925.2:n.2186-4867A>G
ENST00000455470.6:c.2432-4867A>G	ENSP00000406565.2:n.2432-4867A>G
ENST00000382292.7:c.9525A>G	ENSP00000371729.3:p.Thr3175=
ENST00000382298.7:c.9525A>G	ENSP00000371735.3:p.Thr3175=
ENST00000402364.1:c.7275A>G	ENSP00000385844.1:p.Thr2425=
ENST00000423156.1:c.1058-4867A>G	ENSP00000390925.1:n.1058-4867A>G
ENST00000455470.5:c.2130-4867A>G
NM_001278055.1:c.9084A>G	NP_001264984.1:p.Thr3028=
NM_014363.5:c.9525A>G	NP_055178.3:p.Thr3175=
XM_005266338.1:c.9552A>G	XP_005266395.1:p.Thr3184=
XM_011535038.1:c.9576A>G	XP_011533340.1:p.Thr3192=
XM_011535039.1:c.9543A>G	XP_011533341.1:p.Thr3181=
XM_005266338.2:c.9552A>G	XP_005266395.1:p.Thr3184=
XM_011535039.2:c.9543A>G	XP_011533341.1:p.Thr3181=
XM_017020539.1:c.9516A>G	XP_016876028.1:p.Thr3172=
XM_024449337.1:c.9552A>G	XP_024305105.1:p.Thr3184=
NM_014363.6:c.9525A>G MANE Select	NP_055178.3:p.Thr3175=
NM_001278055.2:c.9084A>G	NP_001264984.1:p.Thr3028=