Canonical Allele Identifier: CA483157444

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23904785A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330646A>T , CM000675.2:g.23330646A>T	GRCh38
NC_000013.10:g.23904785A>T , CM000675.1:g.23904785A>T	GRCh37
NC_000013.9:g.22802785A>T	NCBI36
NG_012342.1:g.108057T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18531T>A	ENSP00000508399.1:n.2186-18531T>A
ENST00000682944.1:c.13257T>A	ENSP00000507173.1:p.Ser4419=
ENST00000683210.1:c.2185+23139T>A	ENSP00000506739.1:n.2185+23139T>A
ENST00000683270.1:c.6446-1162T>A	ENSP00000507624.1:n.6446-1162T>A
ENST00000683367.1:c.2177-1162T>A	ENSP00000507780.1:n.2177-1162T>A
ENST00000683489.1:c.2292-694T>A	ENSP00000508403.1:n.2292-694T>A
ENST00000683680.1:c.2319-694T>A	ENSP00000507223.1:n.2319-694T>A
ENST00000684163.1:c.2204-1162T>A	ENSP00000508262.1:n.2204-1162T>A
ENST00000684196.1:n.4543-1162T>A
ENST00000684325.1:c.2186-8972T>A	ENSP00000508121.1:n.2186-8972T>A
ENST00000684385.1:c.2221-1162T>A	ENSP00000507855.1:n.2221-1162T>A
ENST00000684497.1:c.2186-8002T>A	ENSP00000507057.1:n.2186-8002T>A
ENST00000382292.9:c.13230T>A MANE Select	ENSP00000371729.3:p.Ser4410=
ENST00000423156.2:c.2186-1162T>A	ENSP00000390925.2:n.2186-1162T>A
ENST00000455470.6:c.2432-1162T>A	ENSP00000406565.2:n.2432-1162T>A
ENST00000382292.7:c.13230T>A	ENSP00000371729.3:p.Ser4410=
ENST00000382298.7:c.13230T>A	ENSP00000371735.3:p.Ser4410=
ENST00000402364.1:c.10980T>A	ENSP00000385844.1:p.Ser3660=
ENST00000423156.1:c.1058-1162T>A	ENSP00000390925.1:n.1058-1162T>A
ENST00000455470.5:c.2130-1162T>A
NM_001278055.1:c.12789T>A	NP_001264984.1:p.Ser4263=
NM_014363.5:c.13230T>A	NP_055178.3:p.Ser4410=
XM_005266338.1:c.13257T>A	XP_005266395.1:p.Ser4419=
XM_011535038.1:c.13281T>A	XP_011533340.1:p.Ser4427=
XM_011535039.1:c.13248T>A	XP_011533341.1:p.Ser4416=
XM_005266338.2:c.13257T>A	XP_005266395.1:p.Ser4419=
XM_011535039.2:c.13248T>A	XP_011533341.1:p.Ser4416=
XM_017020539.1:c.13221T>A	XP_016876028.1:p.Ser4407=
XM_024449337.1:c.13257T>A	XP_024305105.1:p.Ser4419=
NM_014363.6:c.13230T>A MANE Select	NP_055178.3:p.Ser4410=
NM_001278055.2:c.12789T>A	NP_001264984.1:p.Ser4263=