Canonical Allele Identifier: CA608985327

Gene: SACS SGCG

Linked Data

• dbSNP Id: rs1485087161
• gnomAD v2: 13-23898777-TG-T
• gnomAD v3: 13-23324638-TG-T
• gnomAD v4: 13-23324638-TG-T
• MyVariant Identifiers: chr13:g.23898778del (hg19) ; chr13:g.23324639del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324641del , CM000675.2:g.23324641del	GRCh38
NC_000013.10:g.23898780del , CM000675.1:g.23898780del	GRCh37
NC_000013.9:g.22796780del	NCBI36
NG_008759.1:g.148721del , LRG_207:g.148721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-12524del (SACS)	ENSP00000508399.1:n.2186-12524del
ENST00000683210.1:c.2185+29146del (SACS)	ENSP00000506739.1:n.2185+29146del
ENST00000684325.1:c.2186-2965del (SACS)	ENSP00000508121.1:n.2186-2965del
ENST00000684497.1:c.2186-1995del (SACS)	ENSP00000507057.1:n.2186-1995del
ENST00000218867.4:c.*100del (SGCG) MANE Select	ENSP00000218867.3:n.*100del
ENST00000218867.3:c.*100del (SGCG)	ENSP00000218867.3:n.*100del
NM_000231.2:c.*100del , LRG_207t1:c.*100del (SGCG)	NP_000222.1:n.*100del
XM_005266505.2:c.*100del (SGCG)	XP_005266562.1:n.*100del
XM_006719861.2:c.*100del (SGCG)	XP_006719924.1:n.*100del
XM_006719861.3:c.*100del (SGCG)	XP_006719924.1:n.*100del
XM_024449397.1:c.*100del (SGCG)	XP_024305165.1:n.*100del
NM_000231.3:c.*100del (SGCG) MANE Select	NP_000222.2:n.*100del
NM_001378244.1:c.*100del (SGCG)	NP_001365173.1:n.*100del
NM_001378245.1:c.*100del (SGCG)	NP_001365174.1:n.*100del
NM_001378246.1:c.*100del (SGCG)	NP_001365175.1:n.*100del