Canonical Allele Identifier: CA2575369400

Gene: SACS SGCG

Linked Data

• gnomAD v4: 13-23324325-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324327del , CM000675.2:g.23324327del	GRCh38
NC_000013.10:g.23898466del , CM000675.1:g.23898466del	GRCh37
NC_000013.9:g.22796466del	NCBI36
NG_008759.1:g.148407del , LRG_207:g.148407del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2186-12211del (SACS)	ENSP00000508399.1:n.2186-12211del
ENST00000683210.1:c.2185+29459del (SACS)	ENSP00000506739.1:n.2185+29459del
ENST00000684325.1:c.2186-2652del (SACS)	ENSP00000508121.1:n.2186-2652del
ENST00000684497.1:c.2186-1682del (SACS)	ENSP00000507057.1:n.2186-1682del
ENST00000218867.4:c.703-41del (SGCG) MANE Select	ENSP00000218867.3:n.703-41del
ENST00000218867.3:c.703-41del (SGCG)	ENSP00000218867.3:n.703-41del
NM_000231.2:c.703-41del , LRG_207t1:c.703-41del (SGCG)	NP_000222.1:n.703-41del
XM_005266505.2:c.703-41del (SGCG)	XP_005266562.1:n.703-41del
XM_006719861.2:c.757-41del (SGCG)	XP_006719924.1:n.757-41del
XM_006719861.3:c.757-41del (SGCG)	XP_006719924.1:n.757-41del
XM_024449397.1:c.703-41del (SGCG)	XP_024305165.1:n.703-41del
NM_000231.3:c.703-41del (SGCG) MANE Select	NP_000222.2:n.703-41del
NM_001378244.1:c.757-41del (SGCG)	NP_001365173.1:n.757-41del
NM_001378245.1:c.703-41del (SGCG)	NP_001365174.1:n.703-41del
NM_001378246.1:c.703-41del (SGCG)	NP_001365175.1:n.703-41del