Canonical Allele Identifier: CA6910959

Gene: SACS

Linked Data

• ClinVar Variation Id: 2056994
• ClinVar RCV Id: RCV002914751
• dbSNP Id: rs777287881
• ExAC: 13:23910840 C / T
• gnomAD v2: 13-23910840-C-T
• gnomAD v4: 13-23336701-C-T
• MyVariant Identifiers: chr13:g.23910840C>T (hg19) ; chr13:g.23336701C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336701C>T , CM000675.2:g.23336701C>T	GRCh38
NC_000013.10:g.23910840C>T , CM000675.1:g.23910840C>T	GRCh37
NC_000013.9:g.22808840C>T	NCBI36
NG_012342.1:g.102002G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+17084G>A	ENSP00000508399.1:n.2185+17084G>A
ENST00000682944.1:c.7202G>A	ENSP00000507173.1:p.Arg2401Lys
ENST00000683210.1:c.2185+17084G>A	ENSP00000506739.1:n.2185+17084G>A
ENST00000683270.1:c.6445+721G>A	ENSP00000507624.1:n.6445+721G>A
ENST00000683367.1:c.2177-7217G>A	ENSP00000507780.1:n.2177-7217G>A
ENST00000683489.1:c.2291+4884G>A	ENSP00000508403.1:n.2291+4884G>A
ENST00000683680.1:c.2318+4884G>A	ENSP00000507223.1:n.2318+4884G>A
ENST00000684163.1:c.2204-7217G>A	ENSP00000508262.1:n.2204-7217G>A
ENST00000684196.1:n.4543-7217G>A
ENST00000684325.1:c.2186-15027G>A	ENSP00000508121.1:n.2186-15027G>A
ENST00000684385.1:c.2221-7217G>A	ENSP00000507855.1:n.2221-7217G>A
ENST00000684497.1:c.2186-14057G>A	ENSP00000507057.1:n.2186-14057G>A
ENST00000382292.9:c.7175G>A MANE Select	ENSP00000371729.3:p.Arg2392Lys
ENST00000423156.2:c.2186-7217G>A	ENSP00000390925.2:n.2186-7217G>A
ENST00000455470.6:c.2431+4744G>A	ENSP00000406565.2:n.2431+4744G>A
ENST00000382292.7:c.7175G>A	ENSP00000371729.3:p.Arg2392Lys
ENST00000382298.7:c.7175G>A	ENSP00000371735.3:p.Arg2392Lys
ENST00000402364.1:c.4925G>A	ENSP00000385844.1:p.Arg1642Lys
ENST00000423156.1:c.1058-7217G>A	ENSP00000390925.1:n.1058-7217G>A
ENST00000455470.5:c.2129+4744G>A
NM_001278055.1:c.6734G>A	NP_001264984.1:p.Arg2245Lys
NM_014363.5:c.7175G>A	NP_055178.3:p.Arg2392Lys
XM_005266338.1:c.7202G>A	XP_005266395.1:p.Arg2401Lys
XM_011535038.1:c.7226G>A	XP_011533340.1:p.Arg2409Lys
XM_011535039.1:c.7193G>A	XP_011533341.1:p.Arg2398Lys
XM_005266338.2:c.7202G>A	XP_005266395.1:p.Arg2401Lys
XM_011535039.2:c.7193G>A	XP_011533341.1:p.Arg2398Lys
XM_017020539.1:c.7166G>A	XP_016876028.1:p.Arg2389Lys
XM_024449337.1:c.7202G>A	XP_024305105.1:p.Arg2401Lys
NM_014363.6:c.7175G>A MANE Select	NP_055178.3:p.Arg2392Lys
NM_001278055.2:c.6734G>A	NP_001264984.1:p.Arg2245Lys