Canonical Allele Identifier: CA483158689

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23907902A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23333763A>G , CM000675.2:g.23333763A>G	GRCh38
NC_000013.10:g.23907902A>G , CM000675.1:g.23907902A>G	GRCh37
NC_000013.9:g.22805902A>G	NCBI36
NG_012342.1:g.104940T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+20022T>C	ENSP00000508399.1:n.2185+20022T>C
ENST00000682944.1:c.10140T>C	ENSP00000507173.1:p.Thr3380=
ENST00000683210.1:c.2185+20022T>C	ENSP00000506739.1:n.2185+20022T>C
ENST00000683270.1:c.6445+3659T>C	ENSP00000507624.1:n.6445+3659T>C
ENST00000683367.1:c.2177-4279T>C	ENSP00000507780.1:n.2177-4279T>C
ENST00000683489.1:c.2292-3811T>C	ENSP00000508403.1:n.2292-3811T>C
ENST00000683680.1:c.2319-3811T>C	ENSP00000507223.1:n.2319-3811T>C
ENST00000684163.1:c.2204-4279T>C	ENSP00000508262.1:n.2204-4279T>C
ENST00000684196.1:n.4543-4279T>C
ENST00000684325.1:c.2186-12089T>C	ENSP00000508121.1:n.2186-12089T>C
ENST00000684385.1:c.2221-4279T>C	ENSP00000507855.1:n.2221-4279T>C
ENST00000684497.1:c.2186-11119T>C	ENSP00000507057.1:n.2186-11119T>C
ENST00000382292.9:c.10113T>C MANE Select	ENSP00000371729.3:p.Thr3371=
ENST00000423156.2:c.2186-4279T>C	ENSP00000390925.2:n.2186-4279T>C
ENST00000455470.6:c.2432-4279T>C	ENSP00000406565.2:n.2432-4279T>C
ENST00000382292.7:c.10113T>C	ENSP00000371729.3:p.Thr3371=
ENST00000382298.7:c.10113T>C	ENSP00000371735.3:p.Thr3371=
ENST00000402364.1:c.7863T>C	ENSP00000385844.1:p.Thr2621=
ENST00000423156.1:c.1058-4279T>C	ENSP00000390925.1:n.1058-4279T>C
ENST00000455470.5:c.2130-4279T>C
NM_001278055.1:c.9672T>C	NP_001264984.1:p.Thr3224=
NM_014363.5:c.10113T>C	NP_055178.3:p.Thr3371=
XM_005266338.1:c.10140T>C	XP_005266395.1:p.Thr3380=
XM_011535038.1:c.10164T>C	XP_011533340.1:p.Thr3388=
XM_011535039.1:c.10131T>C	XP_011533341.1:p.Thr3377=
XM_005266338.2:c.10140T>C	XP_005266395.1:p.Thr3380=
XM_011535039.2:c.10131T>C	XP_011533341.1:p.Thr3377=
XM_017020539.1:c.10104T>C	XP_016876028.1:p.Thr3368=
XM_024449337.1:c.10140T>C	XP_024305105.1:p.Thr3380=
NM_014363.6:c.10113T>C MANE Select	NP_055178.3:p.Thr3371=
NM_001278055.2:c.9672T>C	NP_001264984.1:p.Thr3224=