Canonical Allele Identifier: CA6910894

Gene: SACS

Linked Data

• ClinVar Variation Id: 2178523
• ClinVar RCV Id: RCV002595581
• dbSNP Id: rs745410019
• ExAC: 13:23910509 T / C
• gnomAD v2: 13-23910509-T-C
• gnomAD v3: 13-23336370-T-C
• gnomAD v4: 13-23336370-T-C
• MyVariant Identifiers: chr13:g.23910509T>C (hg19) ; chr13:g.23336370T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23336370T>C , CM000675.2:g.23336370T>C	GRCh38
NC_000013.10:g.23910509T>C , CM000675.1:g.23910509T>C	GRCh37
NC_000013.9:g.22808509T>C	NCBI36
NG_012342.1:g.102333A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+17415A>G	ENSP00000508399.1:n.2185+17415A>G
ENST00000682944.1:c.7533A>G	ENSP00000507173.1:p.Arg2511=
ENST00000683210.1:c.2185+17415A>G	ENSP00000506739.1:n.2185+17415A>G
ENST00000683270.1:c.6445+1052A>G	ENSP00000507624.1:n.6445+1052A>G
ENST00000683367.1:c.2177-6886A>G	ENSP00000507780.1:n.2177-6886A>G
ENST00000683489.1:c.2291+5215A>G	ENSP00000508403.1:n.2291+5215A>G
ENST00000683680.1:c.2318+5215A>G	ENSP00000507223.1:n.2318+5215A>G
ENST00000684163.1:c.2204-6886A>G	ENSP00000508262.1:n.2204-6886A>G
ENST00000684196.1:n.4543-6886A>G
ENST00000684325.1:c.2186-14696A>G	ENSP00000508121.1:n.2186-14696A>G
ENST00000684385.1:c.2221-6886A>G	ENSP00000507855.1:n.2221-6886A>G
ENST00000684497.1:c.2186-13726A>G	ENSP00000507057.1:n.2186-13726A>G
ENST00000382292.9:c.7506A>G MANE Select	ENSP00000371729.3:p.Arg2502=
ENST00000423156.2:c.2186-6886A>G	ENSP00000390925.2:n.2186-6886A>G
ENST00000455470.6:c.2431+5075A>G	ENSP00000406565.2:n.2431+5075A>G
ENST00000382292.7:c.7506A>G	ENSP00000371729.3:p.Arg2502=
ENST00000382298.7:c.7506A>G	ENSP00000371735.3:p.Arg2502=
ENST00000402364.1:c.5256A>G	ENSP00000385844.1:p.Arg1752=
ENST00000423156.1:c.1058-6886A>G	ENSP00000390925.1:n.1058-6886A>G
ENST00000455470.5:c.2129+5075A>G
NM_001278055.1:c.7065A>G	NP_001264984.1:p.Arg2355=
NM_014363.5:c.7506A>G	NP_055178.3:p.Arg2502=
XM_005266338.1:c.7533A>G	XP_005266395.1:p.Arg2511=
XM_011535038.1:c.7557A>G	XP_011533340.1:p.Arg2519=
XM_011535039.1:c.7524A>G	XP_011533341.1:p.Arg2508=
XM_005266338.2:c.7533A>G	XP_005266395.1:p.Arg2511=
XM_011535039.2:c.7524A>G	XP_011533341.1:p.Arg2508=
XM_017020539.1:c.7497A>G	XP_016876028.1:p.Arg2499=
XM_024449337.1:c.7533A>G	XP_024305105.1:p.Arg2511=
NM_014363.6:c.7506A>G MANE Select	NP_055178.3:p.Arg2502=
NM_001278055.2:c.7065A>G	NP_001264984.1:p.Arg2355=