Canonical Allele Identifier: CA482918187

Gene: SACS SGCG

Linked Data

• MyVariant Identifiers: chr13:g.23898566C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324427C>T , CM000675.2:g.23324427C>T	GRCh38
NC_000013.10:g.23898566C>T , CM000675.1:g.23898566C>T	GRCh37
NC_000013.9:g.22796566C>T	NCBI36
NG_008759.1:g.148507C>T , LRG_207:g.148507C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-12312G>A (SACS)	ENSP00000508399.1:n.2186-12312G>A
ENST00000683210.1:c.2185+29358G>A (SACS)	ENSP00000506739.1:n.2185+29358G>A
ENST00000684325.1:c.2186-2753G>A (SACS)	ENSP00000508121.1:n.2186-2753G>A
ENST00000684497.1:c.2186-1783G>A (SACS)	ENSP00000507057.1:n.2186-1783G>A
ENST00000218867.4:c.762C>T (SGCG) MANE Select	ENSP00000218867.3:p.Pro254=
ENST00000218867.3:c.762C>T (SGCG)	ENSP00000218867.3:p.Pro254=
NM_000231.2:c.762C>T , LRG_207t1:c.762C>T (SGCG)	NP_000222.1:p.Pro254=
XM_005266505.2:c.762C>T (SGCG)	XP_005266562.1:p.Pro254=
XM_006719861.2:c.816C>T (SGCG)	XP_006719924.1:p.Pro272=
XM_006719861.3:c.816C>T (SGCG)	XP_006719924.1:p.Pro272=
XM_024449397.1:c.762C>T (SGCG)	XP_024305165.1:p.Pro254=
NM_000231.3:c.762C>T (SGCG) MANE Select	NP_000222.2:p.Pro254=
NM_001378244.1:c.816C>T (SGCG)	NP_001365173.1:p.Pro272=
NM_001378245.1:c.762C>T (SGCG)	NP_001365174.1:p.Pro254=
NM_001378246.1:c.762C>T (SGCG)	NP_001365175.1:p.Pro254=