Canonical Allele Identifier: CA387515286

Gene: SACS

Linked Data

• ClinVar Variation Id: 1209834
• ClinVar RCV Id: RCV001579253
• dbSNP Id: rs2137587151
• MyVariant Identifiers: chr13:g.23908960T>C (hg19) ; chr13:g.23334821T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334821T>C , CM000675.2:g.23334821T>C	GRCh38
NC_000013.10:g.23908960T>C , CM000675.1:g.23908960T>C	GRCh37
NC_000013.9:g.22806960T>C	NCBI36
NG_012342.1:g.103882A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18964A>G	ENSP00000508399.1:n.2185+18964A>G
ENST00000682944.1:c.9082A>G	ENSP00000507173.1:p.Thr3028Ala
ENST00000683210.1:c.2185+18964A>G	ENSP00000506739.1:n.2185+18964A>G
ENST00000683270.1:c.6445+2601A>G	ENSP00000507624.1:n.6445+2601A>G
ENST00000683367.1:c.2177-5337A>G	ENSP00000507780.1:n.2177-5337A>G
ENST00000683489.1:c.2292-4869A>G	ENSP00000508403.1:n.2292-4869A>G
ENST00000683680.1:c.2319-4869A>G	ENSP00000507223.1:n.2319-4869A>G
ENST00000684163.1:c.2204-5337A>G	ENSP00000508262.1:n.2204-5337A>G
ENST00000684196.1:n.4543-5337A>G
ENST00000684325.1:c.2186-13147A>G	ENSP00000508121.1:n.2186-13147A>G
ENST00000684385.1:c.2221-5337A>G	ENSP00000507855.1:n.2221-5337A>G
ENST00000684497.1:c.2186-12177A>G	ENSP00000507057.1:n.2186-12177A>G
ENST00000382292.9:c.9055A>G MANE Select	ENSP00000371729.3:p.Thr3019Ala
ENST00000423156.2:c.2186-5337A>G	ENSP00000390925.2:n.2186-5337A>G
ENST00000455470.6:c.2432-5337A>G	ENSP00000406565.2:n.2432-5337A>G
ENST00000382292.7:c.9055A>G	ENSP00000371729.3:p.Thr3019Ala
ENST00000382298.7:c.9055A>G	ENSP00000371735.3:p.Thr3019Ala
ENST00000402364.1:c.6805A>G	ENSP00000385844.1:p.Thr2269Ala
ENST00000423156.1:c.1058-5337A>G	ENSP00000390925.1:n.1058-5337A>G
ENST00000455470.5:c.2130-5337A>G
NM_001278055.1:c.8614A>G	NP_001264984.1:p.Thr2872Ala
NM_014363.5:c.9055A>G	NP_055178.3:p.Thr3019Ala
XM_005266338.1:c.9082A>G	XP_005266395.1:p.Thr3028Ala
XM_011535038.1:c.9106A>G	XP_011533340.1:p.Thr3036Ala
XM_011535039.1:c.9073A>G	XP_011533341.1:p.Thr3025Ala
XM_005266338.2:c.9082A>G	XP_005266395.1:p.Thr3028Ala
XM_011535039.2:c.9073A>G	XP_011533341.1:p.Thr3025Ala
XM_017020539.1:c.9046A>G	XP_016876028.1:p.Thr3016Ala
XM_024449337.1:c.9082A>G	XP_024305105.1:p.Thr3028Ala
NM_014363.6:c.9055A>G MANE Select	NP_055178.3:p.Thr3019Ala
NM_001278055.2:c.8614A>G	NP_001264984.1:p.Thr2872Ala