Canonical Allele Identifier: CA387520091

Gene: SACS

Linked Data

• ClinVar Variation Id: 2081803
• ClinVar RCV Id: RCV002995629
• MyVariant Identifiers: chr13:g.23910936G>T (hg19) ; chr13:g.23336797G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336797G>T , CM000675.2:g.23336797G>T	GRCh38
NC_000013.10:g.23910936G>T , CM000675.1:g.23910936G>T	GRCh37
NC_000013.9:g.22808936G>T	NCBI36
NG_012342.1:g.101906C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+16988C>A	ENSP00000508399.1:n.2185+16988C>A
ENST00000682944.1:c.7106C>A	ENSP00000507173.1:p.Ser2369Tyr
ENST00000683210.1:c.2185+16988C>A	ENSP00000506739.1:n.2185+16988C>A
ENST00000683270.1:c.6445+625C>A	ENSP00000507624.1:n.6445+625C>A
ENST00000683367.1:c.2177-7313C>A	ENSP00000507780.1:n.2177-7313C>A
ENST00000683489.1:c.2291+4788C>A	ENSP00000508403.1:n.2291+4788C>A
ENST00000683680.1:c.2318+4788C>A	ENSP00000507223.1:n.2318+4788C>A
ENST00000684163.1:c.2204-7313C>A	ENSP00000508262.1:n.2204-7313C>A
ENST00000684196.1:n.4543-7313C>A
ENST00000684325.1:c.2186-15123C>A	ENSP00000508121.1:n.2186-15123C>A
ENST00000684385.1:c.2221-7313C>A	ENSP00000507855.1:n.2221-7313C>A
ENST00000684497.1:c.2186-14153C>A	ENSP00000507057.1:n.2186-14153C>A
ENST00000382292.9:c.7079C>A MANE Select	ENSP00000371729.3:p.Ser2360Tyr
ENST00000423156.2:c.2186-7313C>A	ENSP00000390925.2:n.2186-7313C>A
ENST00000455470.6:c.2431+4648C>A	ENSP00000406565.2:n.2431+4648C>A
ENST00000382292.7:c.7079C>A	ENSP00000371729.3:p.Ser2360Tyr
ENST00000382298.7:c.7079C>A	ENSP00000371735.3:p.Ser2360Tyr
ENST00000402364.1:c.4829C>A	ENSP00000385844.1:p.Ser1610Tyr
ENST00000423156.1:c.1058-7313C>A	ENSP00000390925.1:n.1058-7313C>A
ENST00000455470.5:c.2129+4648C>A
NM_001278055.1:c.6638C>A	NP_001264984.1:p.Ser2213Tyr
NM_014363.5:c.7079C>A	NP_055178.3:p.Ser2360Tyr
XM_005266338.1:c.7106C>A	XP_005266395.1:p.Ser2369Tyr
XM_011535038.1:c.7130C>A	XP_011533340.1:p.Ser2377Tyr
XM_011535039.1:c.7097C>A	XP_011533341.1:p.Ser2366Tyr
XM_005266338.2:c.7106C>A	XP_005266395.1:p.Ser2369Tyr
XM_011535039.2:c.7097C>A	XP_011533341.1:p.Ser2366Tyr
XM_017020539.1:c.7070C>A	XP_016876028.1:p.Ser2357Tyr
XM_024449337.1:c.7106C>A	XP_024305105.1:p.Ser2369Tyr
NM_014363.6:c.7079C>A MANE Select	NP_055178.3:p.Ser2360Tyr
NM_001278055.2:c.6638C>A	NP_001264984.1:p.Ser2213Tyr