Canonical Allele Identifier: CA6909824

Gene: SACS SGCG

Linked Data

• dbSNP Id: rs369980849
• ExAC: 13:23898461 G / A
• gnomAD v2: 13-23898461-G-A
• gnomAD v3: 13-23324322-G-A
• gnomAD v4: 13-23324322-G-A
• MyVariant Identifiers: chr13:g.23898461G>A (hg19) ; chr13:g.23324322G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324322G>A , CM000675.2:g.23324322G>A	GRCh38
NC_000013.10:g.23898461G>A , CM000675.1:g.23898461G>A	GRCh37
NC_000013.9:g.22796461G>A	NCBI36
NG_008759.1:g.148402G>A , LRG_207:g.148402G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-12207C>T (SACS)	ENSP00000508399.1:n.2186-12207C>T
ENST00000683210.1:c.2185+29463C>T (SACS)	ENSP00000506739.1:n.2185+29463C>T
ENST00000684325.1:c.2186-2648C>T (SACS)	ENSP00000508121.1:n.2186-2648C>T
ENST00000684497.1:c.2186-1678C>T (SACS)	ENSP00000507057.1:n.2186-1678C>T
ENST00000218867.4:c.703-46G>A (SGCG) MANE Select	ENSP00000218867.3:n.703-46G>A
ENST00000218867.3:c.703-46G>A (SGCG)	ENSP00000218867.3:n.703-46G>A
NM_000231.2:c.703-46G>A , LRG_207t1:c.703-46G>A (SGCG)	NP_000222.1:n.703-46G>A
XM_005266505.2:c.703-46G>A (SGCG)	XP_005266562.1:n.703-46G>A
XM_006719861.2:c.757-46G>A (SGCG)	XP_006719924.1:n.757-46G>A
XM_006719861.3:c.757-46G>A (SGCG)	XP_006719924.1:n.757-46G>A
XM_024449397.1:c.703-46G>A (SGCG)	XP_024305165.1:n.703-46G>A
NM_000231.3:c.703-46G>A (SGCG) MANE Select	NP_000222.2:n.703-46G>A
NM_001378244.1:c.757-46G>A (SGCG)	NP_001365173.1:n.757-46G>A
NM_001378245.1:c.703-46G>A (SGCG)	NP_001365174.1:n.703-46G>A
NM_001378246.1:c.703-46G>A (SGCG)	NP_001365175.1:n.703-46G>A