Canonical Allele Identifier: CA6910361

Gene: SACS

Linked Data

• ClinVar Variation Id: 260390
• ClinVar RCV Id: RCV000248252 ; RCV000868348 ; RCV001288374
• dbSNP Id: rs115155117
• ExAC: 13:23907043 G / A
• gnomAD v2: 13-23907043-G-A
• gnomAD v3: 13-23332904-G-A
• gnomAD v4: 13-23332904-G-A
• MyVariant Identifiers: chr13:g.23907043G>A (hg19) ; chr13:g.23332904G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23332904G>A , CM000675.2:g.23332904G>A	GRCh38
NC_000013.10:g.23907043G>A , CM000675.1:g.23907043G>A	GRCh37
NC_000013.9:g.22805043G>A	NCBI36
NG_012342.1:g.105799C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-20789C>T	ENSP00000508399.1:n.2186-20789C>T
ENST00000682944.1:c.10999C>T	ENSP00000507173.1:p.Arg3667Trp
ENST00000683210.1:c.2185+20881C>T	ENSP00000506739.1:n.2185+20881C>T
ENST00000683270.1:c.6446-3420C>T	ENSP00000507624.1:n.6446-3420C>T
ENST00000683367.1:c.2177-3420C>T	ENSP00000507780.1:n.2177-3420C>T
ENST00000683489.1:c.2292-2952C>T	ENSP00000508403.1:n.2292-2952C>T
ENST00000683680.1:c.2319-2952C>T	ENSP00000507223.1:n.2319-2952C>T
ENST00000684163.1:c.2204-3420C>T	ENSP00000508262.1:n.2204-3420C>T
ENST00000684196.1:n.4543-3420C>T
ENST00000684325.1:c.2186-11230C>T	ENSP00000508121.1:n.2186-11230C>T
ENST00000684385.1:c.2221-3420C>T	ENSP00000507855.1:n.2221-3420C>T
ENST00000684497.1:c.2186-10260C>T	ENSP00000507057.1:n.2186-10260C>T
ENST00000382292.9:c.10972C>T MANE Select	ENSP00000371729.3:p.Arg3658Trp
ENST00000423156.2:c.2186-3420C>T	ENSP00000390925.2:n.2186-3420C>T
ENST00000455470.6:c.2432-3420C>T	ENSP00000406565.2:n.2432-3420C>T
ENST00000382292.7:c.10972C>T	ENSP00000371729.3:p.Arg3658Trp
ENST00000382298.7:c.10972C>T	ENSP00000371735.3:p.Arg3658Trp
ENST00000402364.1:c.8722C>T	ENSP00000385844.1:p.Arg2908Trp
ENST00000423156.1:c.1058-3420C>T	ENSP00000390925.1:n.1058-3420C>T
ENST00000455470.5:c.2130-3420C>T
NM_001278055.1:c.10531C>T	NP_001264984.1:p.Arg3511Trp
NM_014363.5:c.10972C>T	NP_055178.3:p.Arg3658Trp
XM_005266338.1:c.10999C>T	XP_005266395.1:p.Arg3667Trp
XM_011535038.1:c.11023C>T	XP_011533340.1:p.Arg3675Trp
XM_011535039.1:c.10990C>T	XP_011533341.1:p.Arg3664Trp
XM_005266338.2:c.10999C>T	XP_005266395.1:p.Arg3667Trp
XM_011535039.2:c.10990C>T	XP_011533341.1:p.Arg3664Trp
XM_017020539.1:c.10963C>T	XP_016876028.1:p.Arg3655Trp
XM_024449337.1:c.10999C>T	XP_024305105.1:p.Arg3667Trp
NM_014363.6:c.10972C>T MANE Select	NP_055178.3:p.Arg3658Trp
NM_001278055.2:c.10531C>T	NP_001264984.1:p.Arg3511Trp