Canonical Allele Identifier: CA6911431

Gene: SACS

Linked Data

• ClinVar Variation Id: 311545
• ClinVar RCV Id: RCV000323040 ; RCV000884011 ; RCV001848103
• dbSNP Id: rs61326562
• ExAC: 13:23913898 C / G
• gnomAD v2: 13-23913898-C-G
• gnomAD v3: 13-23339759-C-G
• gnomAD v4: 13-23339759-C-G
• MyVariant Identifiers: chr13:g.23913898C>G (hg19) ; chr13:g.23339759C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23339759C>G , CM000675.2:g.23339759C>G	GRCh38
NC_000013.10:g.23913898C>G , CM000675.1:g.23913898C>G	GRCh37
NC_000013.9:g.22811898C>G	NCBI36
NG_012342.1:g.98944G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+14026G>C	ENSP00000508399.1:n.2185+14026G>C
ENST00000682944.1:c.4144G>C	ENSP00000507173.1:p.Ala1382Pro
ENST00000683210.1:c.2185+14026G>C	ENSP00000506739.1:n.2185+14026G>C
ENST00000683270.1:c.4108G>C	ENSP00000507624.1:p.Ala1370Pro
ENST00000683367.1:c.2177-10275G>C	ENSP00000507780.1:n.2177-10275G>C
ENST00000683489.1:c.2291+1826G>C	ENSP00000508403.1:n.2291+1826G>C
ENST00000683680.1:c.2318+1826G>C	ENSP00000507223.1:n.2318+1826G>C
ENST00000684163.1:c.2203+7052G>C	ENSP00000508262.1:n.2203+7052G>C
ENST00000684196.1:n.4543-10275G>C
ENST00000684325.1:c.2185+14026G>C	ENSP00000508121.1:n.2185+14026G>C
ENST00000684385.1:c.2220+7052G>C	ENSP00000507855.1:n.2220+7052G>C
ENST00000684497.1:c.2185+14026G>C	ENSP00000507057.1:n.2185+14026G>C
ENST00000382292.9:c.4117G>C MANE Select	ENSP00000371729.3:p.Ala1373Pro
ENST00000423156.2:c.2186-10275G>C	ENSP00000390925.2:n.2186-10275G>C
ENST00000455470.6:c.2431+1686G>C	ENSP00000406565.2:n.2431+1686G>C
ENST00000382292.7:c.4117G>C	ENSP00000371729.3:p.Ala1373Pro
ENST00000382298.7:c.4117G>C	ENSP00000371735.3:p.Ala1373Pro
ENST00000402364.1:c.1867G>C	ENSP00000385844.1:p.Ala623Pro
ENST00000423156.1:c.1058-10275G>C	ENSP00000390925.1:n.1058-10275G>C
ENST00000455470.5:c.2129+1686G>C
NM_001278055.1:c.3676G>C	NP_001264984.1:p.Ala1226Pro
NM_014363.5:c.4117G>C	NP_055178.3:p.Ala1373Pro
XM_005266338.1:c.4144G>C	XP_005266395.1:p.Ala1382Pro
XM_011535038.1:c.4168G>C	XP_011533340.1:p.Ala1390Pro
XM_011535039.1:c.4135G>C	XP_011533341.1:p.Ala1379Pro
XM_005266338.2:c.4144G>C	XP_005266395.1:p.Ala1382Pro
XM_011535039.2:c.4135G>C	XP_011533341.1:p.Ala1379Pro
XM_017020539.1:c.4108G>C	XP_016876028.1:p.Ala1370Pro
XM_024449337.1:c.4144G>C	XP_024305105.1:p.Ala1382Pro
NM_014363.6:c.4117G>C MANE Select	NP_055178.3:p.Ala1373Pro
NM_001278055.2:c.3676G>C	NP_001264984.1:p.Ala1226Pro