Canonical Allele Identifier: CA387503631

Gene: SACS SGCG

Linked Data

• MyVariant Identifiers: chr13:g.23898556C>G (hg19) ; chr13:g.23324417C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324417C>G , CM000675.2:g.23324417C>G	GRCh38
NC_000013.10:g.23898556C>G , CM000675.1:g.23898556C>G	GRCh37
NC_000013.9:g.22796556C>G	NCBI36
NG_008759.1:g.148497C>G , LRG_207:g.148497C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-12302G>C (SACS)	ENSP00000508399.1:n.2186-12302G>C
ENST00000683210.1:c.2185+29368G>C (SACS)	ENSP00000506739.1:n.2185+29368G>C
ENST00000684325.1:c.2186-2743G>C (SACS)	ENSP00000508121.1:n.2186-2743G>C
ENST00000684497.1:c.2186-1773G>C (SACS)	ENSP00000507057.1:n.2186-1773G>C
ENST00000218867.4:c.752C>G (SGCG) MANE Select	ENSP00000218867.3:p.Thr251Arg
ENST00000218867.3:c.752C>G (SGCG)	ENSP00000218867.3:p.Thr251Arg
NM_000231.2:c.752C>G , LRG_207t1:c.752C>G (SGCG)	NP_000222.1:p.Thr251Arg
XM_005266505.2:c.752C>G (SGCG)	XP_005266562.1:p.Thr251Arg
XM_006719861.2:c.806C>G (SGCG)	XP_006719924.1:p.Thr269Arg
XM_006719861.3:c.806C>G (SGCG)	XP_006719924.1:p.Thr269Arg
XM_024449397.1:c.752C>G (SGCG)	XP_024305165.1:p.Thr251Arg
NM_000231.3:c.752C>G (SGCG) MANE Select	NP_000222.2:p.Thr251Arg
NM_001378244.1:c.806C>G (SGCG)	NP_001365173.1:p.Thr269Arg
NM_001378245.1:c.752C>G (SGCG)	NP_001365174.1:p.Thr251Arg
NM_001378246.1:c.752C>G (SGCG)	NP_001365175.1:p.Thr251Arg