Canonical Allele Identifier: CA2622327779

Gene: SACS SGCG

Linked Data

• gnomAD v4: 13-23324411-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324415dup , CM000675.2:g.23324415dup	GRCh38
NC_000013.10:g.23898554dup , CM000675.1:g.23898554dup	GRCh37
NC_000013.9:g.22796554dup	NCBI36
NG_008759.1:g.148495dup , LRG_207:g.148495dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-12297dup (SACS)	ENSP00000508399.1:n.2186-12297dup
ENST00000683210.1:c.2185+29373dup (SACS)	ENSP00000506739.1:n.2185+29373dup
ENST00000684325.1:c.2186-2738dup (SACS)	ENSP00000508121.1:n.2186-2738dup
ENST00000684497.1:c.2186-1768dup (SACS)	ENSP00000507057.1:n.2186-1768dup
ENST00000218867.4:c.750dup (SGCG) MANE Select	ENSP00000218867.3:p.Thr251AspfsTer?
ENST00000218867.3:c.750dup (SGCG)	ENSP00000218867.3:p.Thr251AspfsTer?
NM_000231.2:c.750dup , LRG_207t1:c.750dup (SGCG)	NP_000222.1:p.Thr251AspfsTer?
XM_005266505.2:c.750dup (SGCG)	XP_005266562.1:p.Thr251AspfsTer?
XM_006719861.2:c.804dup (SGCG)	XP_006719924.1:p.Thr269AspfsTer?
XM_006719861.3:c.804dup (SGCG)	XP_006719924.1:p.Thr269AspfsTer?
XM_024449397.1:c.750dup (SGCG)	XP_024305165.1:p.Thr251AspfsTer?
NM_000231.3:c.750dup (SGCG) MANE Select	NP_000222.2:p.Thr251AspfsTer?
NM_001378244.1:c.804dup (SGCG)	NP_001365173.1:p.Thr269AspfsTer?
NM_001378245.1:c.750dup (SGCG)	NP_001365174.1:p.Thr251AspfsTer?
NM_001378246.1:c.750dup (SGCG)	NP_001365175.1:p.Thr251AspfsTer?