Canonical Allele Identifier: CA6909863

Gene: SACS SGCG

Linked Data

• ClinVar Variation Id: 1643740
• ClinVar RCV Id: RCV002145938
• dbSNP Id: rs778036404
• ExAC: 13:23898650 G / A
• gnomAD v2: 13-23898650-G-A
• gnomAD v4: 13-23324511-G-A
• MyVariant Identifiers: chr13:g.23898650G>A (hg19) ; chr13:g.23324511G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324511G>A , CM000675.2:g.23324511G>A	GRCh38
NC_000013.10:g.23898650G>A , CM000675.1:g.23898650G>A	GRCh37
NC_000013.9:g.22796650G>A	NCBI36
NG_008759.1:g.148591G>A , LRG_207:g.148591G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-12396C>T (SACS)	ENSP00000508399.1:n.2186-12396C>T
ENST00000683210.1:c.2185+29274C>T (SACS)	ENSP00000506739.1:n.2185+29274C>T
ENST00000684325.1:c.2186-2837C>T (SACS)	ENSP00000508121.1:n.2186-2837C>T
ENST00000684497.1:c.2186-1867C>T (SACS)	ENSP00000507057.1:n.2186-1867C>T
ENST00000218867.4:c.846G>A (SGCG) MANE Select	ENSP00000218867.3:p.Thr282=
ENST00000218867.3:c.846G>A (SGCG)	ENSP00000218867.3:p.Thr282=
NM_000231.2:c.846G>A , LRG_207t1:c.846G>A (SGCG)	NP_000222.1:p.Thr282=
XM_005266505.2:c.846G>A (SGCG)	XP_005266562.1:p.Thr282=
XM_006719861.2:c.900G>A (SGCG)	XP_006719924.1:p.Thr300=
XM_006719861.3:c.900G>A (SGCG)	XP_006719924.1:p.Thr300=
XM_024449397.1:c.846G>A (SGCG)	XP_024305165.1:p.Thr282=
NM_000231.3:c.846G>A (SGCG) MANE Select	NP_000222.2:p.Thr282=
NM_001378244.1:c.900G>A (SGCG)	NP_001365173.1:p.Thr300=
NM_001378245.1:c.846G>A (SGCG)	NP_001365174.1:p.Thr282=
NM_001378246.1:c.846G>A (SGCG)	NP_001365175.1:p.Thr282=