Canonical Allele Identifier: CA483160035

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23909221G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23335082G>T , CM000675.2:g.23335082G>T	GRCh38
NC_000013.10:g.23909221G>T , CM000675.1:g.23909221G>T	GRCh37
NC_000013.9:g.22807221G>T	NCBI36
NG_012342.1:g.103621C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+18703C>A	ENSP00000508399.1:n.2185+18703C>A
ENST00000682944.1:c.8821C>A	ENSP00000507173.1:p.Arg2941=
ENST00000683210.1:c.2185+18703C>A	ENSP00000506739.1:n.2185+18703C>A
ENST00000683270.1:c.6445+2340C>A	ENSP00000507624.1:n.6445+2340C>A
ENST00000683367.1:c.2177-5598C>A	ENSP00000507780.1:n.2177-5598C>A
ENST00000683489.1:c.2292-5130C>A	ENSP00000508403.1:n.2292-5130C>A
ENST00000683680.1:c.2319-5130C>A	ENSP00000507223.1:n.2319-5130C>A
ENST00000684163.1:c.2204-5598C>A	ENSP00000508262.1:n.2204-5598C>A
ENST00000684196.1:n.4543-5598C>A
ENST00000684325.1:c.2186-13408C>A	ENSP00000508121.1:n.2186-13408C>A
ENST00000684385.1:c.2221-5598C>A	ENSP00000507855.1:n.2221-5598C>A
ENST00000684497.1:c.2186-12438C>A	ENSP00000507057.1:n.2186-12438C>A
ENST00000382292.9:c.8794C>A MANE Select	ENSP00000371729.3:p.Arg2932=
ENST00000423156.2:c.2186-5598C>A	ENSP00000390925.2:n.2186-5598C>A
ENST00000455470.6:c.2432-5598C>A	ENSP00000406565.2:n.2432-5598C>A
ENST00000382292.7:c.8794C>A	ENSP00000371729.3:p.Arg2932=
ENST00000382298.7:c.8794C>A	ENSP00000371735.3:p.Arg2932=
ENST00000402364.1:c.6544C>A	ENSP00000385844.1:p.Arg2182=
ENST00000423156.1:c.1058-5598C>A	ENSP00000390925.1:n.1058-5598C>A
ENST00000455470.5:c.2130-5598C>A
NM_001278055.1:c.8353C>A	NP_001264984.1:p.Arg2785=
NM_014363.5:c.8794C>A	NP_055178.3:p.Arg2932=
XM_005266338.1:c.8821C>A	XP_005266395.1:p.Arg2941=
XM_011535038.1:c.8845C>A	XP_011533340.1:p.Arg2949=
XM_011535039.1:c.8812C>A	XP_011533341.1:p.Arg2938=
XM_005266338.2:c.8821C>A	XP_005266395.1:p.Arg2941=
XM_011535039.2:c.8812C>A	XP_011533341.1:p.Arg2938=
XM_017020539.1:c.8785C>A	XP_016876028.1:p.Arg2929=
XM_024449337.1:c.8821C>A	XP_024305105.1:p.Arg2941=
NM_014363.6:c.8794C>A MANE Select	NP_055178.3:p.Arg2932=
NM_001278055.2:c.8353C>A	NP_001264984.1:p.Arg2785=