Canonical Allele Identifier: CA387510844

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23906962C>T (hg19) ; chr13:g.23332823C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23332823C>T , CM000675.2:g.23332823C>T	GRCh38
NC_000013.10:g.23906962C>T , CM000675.1:g.23906962C>T	GRCh37
NC_000013.9:g.22804962C>T	NCBI36
NG_012342.1:g.105880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-20708G>A	ENSP00000508399.1:n.2186-20708G>A
ENST00000682944.1:c.11080G>A	ENSP00000507173.1:p.Ala3694Thr
ENST00000683210.1:c.2185+20962G>A	ENSP00000506739.1:n.2185+20962G>A
ENST00000683270.1:c.6446-3339G>A	ENSP00000507624.1:n.6446-3339G>A
ENST00000683367.1:c.2177-3339G>A	ENSP00000507780.1:n.2177-3339G>A
ENST00000683489.1:c.2292-2871G>A	ENSP00000508403.1:n.2292-2871G>A
ENST00000683680.1:c.2319-2871G>A	ENSP00000507223.1:n.2319-2871G>A
ENST00000684163.1:c.2204-3339G>A	ENSP00000508262.1:n.2204-3339G>A
ENST00000684196.1:n.4543-3339G>A
ENST00000684325.1:c.2186-11149G>A	ENSP00000508121.1:n.2186-11149G>A
ENST00000684385.1:c.2221-3339G>A	ENSP00000507855.1:n.2221-3339G>A
ENST00000684497.1:c.2186-10179G>A	ENSP00000507057.1:n.2186-10179G>A
ENST00000382292.9:c.11053G>A MANE Select	ENSP00000371729.3:p.Ala3685Thr
ENST00000423156.2:c.2186-3339G>A	ENSP00000390925.2:n.2186-3339G>A
ENST00000455470.6:c.2432-3339G>A	ENSP00000406565.2:n.2432-3339G>A
ENST00000382292.7:c.11053G>A	ENSP00000371729.3:p.Ala3685Thr
ENST00000382298.7:c.11053G>A	ENSP00000371735.3:p.Ala3685Thr
ENST00000402364.1:c.8803G>A	ENSP00000385844.1:p.Ala2935Thr
ENST00000423156.1:c.1058-3339G>A	ENSP00000390925.1:n.1058-3339G>A
ENST00000455470.5:c.2130-3339G>A
NM_001278055.1:c.10612G>A	NP_001264984.1:p.Ala3538Thr
NM_014363.5:c.11053G>A	NP_055178.3:p.Ala3685Thr
XM_005266338.1:c.11080G>A	XP_005266395.1:p.Ala3694Thr
XM_011535038.1:c.11104G>A	XP_011533340.1:p.Ala3702Thr
XM_011535039.1:c.11071G>A	XP_011533341.1:p.Ala3691Thr
XM_005266338.2:c.11080G>A	XP_005266395.1:p.Ala3694Thr
XM_011535039.2:c.11071G>A	XP_011533341.1:p.Ala3691Thr
XM_017020539.1:c.11044G>A	XP_016876028.1:p.Ala3682Thr
XM_024449337.1:c.11080G>A	XP_024305105.1:p.Ala3694Thr
NM_014363.6:c.11053G>A MANE Select	NP_055178.3:p.Ala3685Thr
NM_001278055.2:c.10612G>A	NP_001264984.1:p.Ala3538Thr