Canonical Allele Identifier: CA6910891

Gene: SACS

Linked Data

• ClinVar Variation Id: 260399
• ClinVar RCV Id: RCV000243536 ; RCV000710207 ; RCV001082626 ; RCV001112102 ; RCV001848029 ; RCV003891946
• dbSNP Id: rs111920492
• ExAC: 13:23910487 C / T
• gnomAD v2: 13-23910487-C-T
• gnomAD v3: 13-23336348-C-T
• gnomAD v4: 13-23336348-C-T
• MyVariant Identifiers: chr13:g.23910487C>T (hg19) ; chr13:g.23336348C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336348C>T , CM000675.2:g.23336348C>T	GRCh38
NC_000013.10:g.23910487C>T , CM000675.1:g.23910487C>T	GRCh37
NC_000013.9:g.22808487C>T	NCBI36
NG_012342.1:g.102355G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+17437G>A	ENSP00000508399.1:n.2185+17437G>A
ENST00000682944.1:c.7555G>A	ENSP00000507173.1:p.Ala2519Thr
ENST00000683210.1:c.2185+17437G>A	ENSP00000506739.1:n.2185+17437G>A
ENST00000683270.1:c.6445+1074G>A	ENSP00000507624.1:n.6445+1074G>A
ENST00000683367.1:c.2177-6864G>A	ENSP00000507780.1:n.2177-6864G>A
ENST00000683489.1:c.2291+5237G>A	ENSP00000508403.1:n.2291+5237G>A
ENST00000683680.1:c.2318+5237G>A	ENSP00000507223.1:n.2318+5237G>A
ENST00000684163.1:c.2204-6864G>A	ENSP00000508262.1:n.2204-6864G>A
ENST00000684196.1:n.4543-6864G>A
ENST00000684325.1:c.2186-14674G>A	ENSP00000508121.1:n.2186-14674G>A
ENST00000684385.1:c.2221-6864G>A	ENSP00000507855.1:n.2221-6864G>A
ENST00000684497.1:c.2186-13704G>A	ENSP00000507057.1:n.2186-13704G>A
ENST00000382292.9:c.7528G>A MANE Select	ENSP00000371729.3:p.Ala2510Thr
ENST00000423156.2:c.2186-6864G>A	ENSP00000390925.2:n.2186-6864G>A
ENST00000455470.6:c.2431+5097G>A	ENSP00000406565.2:n.2431+5097G>A
ENST00000382292.7:c.7528G>A	ENSP00000371729.3:p.Ala2510Thr
ENST00000382298.7:c.7528G>A	ENSP00000371735.3:p.Ala2510Thr
ENST00000402364.1:c.5278G>A	ENSP00000385844.1:p.Ala1760Thr
ENST00000423156.1:c.1058-6864G>A	ENSP00000390925.1:n.1058-6864G>A
ENST00000455470.5:c.2129+5097G>A
NM_001278055.1:c.7087G>A	NP_001264984.1:p.Ala2363Thr
NM_014363.5:c.7528G>A	NP_055178.3:p.Ala2510Thr
XM_005266338.1:c.7555G>A	XP_005266395.1:p.Ala2519Thr
XM_011535038.1:c.7579G>A	XP_011533340.1:p.Ala2527Thr
XM_011535039.1:c.7546G>A	XP_011533341.1:p.Ala2516Thr
XM_005266338.2:c.7555G>A	XP_005266395.1:p.Ala2519Thr
XM_011535039.2:c.7546G>A	XP_011533341.1:p.Ala2516Thr
XM_017020539.1:c.7519G>A	XP_016876028.1:p.Ala2507Thr
XM_024449337.1:c.7555G>A	XP_024305105.1:p.Ala2519Thr
NM_014363.6:c.7528G>A MANE Select	NP_055178.3:p.Ala2510Thr
NM_001278055.2:c.7087G>A	NP_001264984.1:p.Ala2363Thr