Canonical Allele Identifier: CA387510774

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23906933A>C (hg19) ; chr13:g.23332794A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23332794A>C , CM000675.2:g.23332794A>C	GRCh38
NC_000013.10:g.23906933A>C , CM000675.1:g.23906933A>C	GRCh37
NC_000013.9:g.22804933A>C	NCBI36
NG_012342.1:g.105909T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-20679T>G	ENSP00000508399.1:n.2186-20679T>G
ENST00000682944.1:c.11109T>G	ENSP00000507173.1:p.Cys3703Trp
ENST00000683210.1:c.2185+20991T>G	ENSP00000506739.1:n.2185+20991T>G
ENST00000683270.1:c.6446-3310T>G	ENSP00000507624.1:n.6446-3310T>G
ENST00000683367.1:c.2177-3310T>G	ENSP00000507780.1:n.2177-3310T>G
ENST00000683489.1:c.2292-2842T>G	ENSP00000508403.1:n.2292-2842T>G
ENST00000683680.1:c.2319-2842T>G	ENSP00000507223.1:n.2319-2842T>G
ENST00000684163.1:c.2204-3310T>G	ENSP00000508262.1:n.2204-3310T>G
ENST00000684196.1:n.4543-3310T>G
ENST00000684325.1:c.2186-11120T>G	ENSP00000508121.1:n.2186-11120T>G
ENST00000684385.1:c.2221-3310T>G	ENSP00000507855.1:n.2221-3310T>G
ENST00000684497.1:c.2186-10150T>G	ENSP00000507057.1:n.2186-10150T>G
ENST00000382292.9:c.11082T>G MANE Select	ENSP00000371729.3:p.Cys3694Trp
ENST00000423156.2:c.2186-3310T>G	ENSP00000390925.2:n.2186-3310T>G
ENST00000455470.6:c.2432-3310T>G	ENSP00000406565.2:n.2432-3310T>G
ENST00000382292.7:c.11082T>G	ENSP00000371729.3:p.Cys3694Trp
ENST00000382298.7:c.11082T>G	ENSP00000371735.3:p.Cys3694Trp
ENST00000402364.1:c.8832T>G	ENSP00000385844.1:p.Cys2944Trp
ENST00000423156.1:c.1058-3310T>G	ENSP00000390925.1:n.1058-3310T>G
ENST00000455470.5:c.2130-3310T>G
NM_001278055.1:c.10641T>G	NP_001264984.1:p.Cys3547Trp
NM_014363.5:c.11082T>G	NP_055178.3:p.Cys3694Trp
XM_005266338.1:c.11109T>G	XP_005266395.1:p.Cys3703Trp
XM_011535038.1:c.11133T>G	XP_011533340.1:p.Cys3711Trp
XM_011535039.1:c.11100T>G	XP_011533341.1:p.Cys3700Trp
XM_005266338.2:c.11109T>G	XP_005266395.1:p.Cys3703Trp
XM_011535039.2:c.11100T>G	XP_011533341.1:p.Cys3700Trp
XM_017020539.1:c.11073T>G	XP_016876028.1:p.Cys3691Trp
XM_024449337.1:c.11109T>G	XP_024305105.1:p.Cys3703Trp
NM_014363.6:c.11082T>G MANE Select	NP_055178.3:p.Cys3694Trp
NM_001278055.2:c.10641T>G	NP_001264984.1:p.Cys3547Trp