Canonical Allele Identifier: CA482922344

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23932583G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23358444G>T , CM000675.2:g.23358444G>T	GRCh38
NC_000013.10:g.23932583G>T , CM000675.1:g.23932583G>T	GRCh37
NC_000013.9:g.22830583G>T	NCBI36
NG_012342.1:g.80259C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.495C>A	ENSP00000508399.1:p.Thr165=
ENST00000682944.1:c.495C>A	ENSP00000507173.1:p.Thr165=
ENST00000683154.1:n.633C>A
ENST00000683210.1:c.495C>A	ENSP00000506739.1:p.Thr165=
ENST00000683270.1:c.486C>A	ENSP00000507624.1:p.Thr162=
ENST00000683367.1:c.486C>A	ENSP00000507780.1:p.Thr162=
ENST00000683489.1:c.495C>A	ENSP00000508403.1:p.Thr165=
ENST00000683680.1:c.495C>A	ENSP00000507223.1:p.Thr165=
ENST00000684163.1:c.486C>A	ENSP00000508262.1:p.Thr162=
ENST00000684196.1:n.2852C>A
ENST00000684325.1:c.495C>A	ENSP00000508121.1:p.Thr165=
ENST00000684385.1:c.495C>A	ENSP00000507855.1:p.Thr165=
ENST00000684497.1:c.495C>A	ENSP00000507057.1:p.Thr165=
ENST00000382292.9:c.495C>A MANE Select	ENSP00000371729.3:p.Thr165=
ENST00000423156.2:c.495C>A	ENSP00000390925.2:p.Thr165=
ENST00000455470.6:c.495C>A	ENSP00000406565.2:p.Thr165=
ENST00000382292.7:c.495C>A	ENSP00000371729.3:p.Thr165=
ENST00000382298.7:c.495C>A	ENSP00000371735.3:p.Thr165=
ENST00000402364.1:c.-1756C>A	ENSP00000385844.1:n.-1756C>A
ENST00000455470.5:c.193C>A
NM_001278055.1:c.54C>A	NP_001264984.1:p.Thr18=
NM_014363.5:c.495C>A	NP_055178.3:p.Thr165=
XM_005266338.1:c.495C>A	XP_005266395.1:p.Thr165=
XM_011535038.1:c.519C>A	XP_011533340.1:p.Thr173=
XM_011535039.1:c.486C>A	XP_011533341.1:p.Thr162=
XM_005266338.2:c.495C>A	XP_005266395.1:p.Thr165=
XM_011535039.2:c.486C>A	XP_011533341.1:p.Thr162=
XM_017020539.1:c.486C>A	XP_016876028.1:p.Thr162=
XM_024449337.1:c.495C>A	XP_024305105.1:p.Thr165=
NM_014363.6:c.495C>A MANE Select	NP_055178.3:p.Thr165=
NM_001278055.2:c.54C>A	NP_001264984.1:p.Thr18=