Canonical Allele Identifier: CA2622327786

Gene: SACS SGCG

Linked Data

• gnomAD v4: 13-23324548-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324550_23324551del , CM000675.2:g.23324550_23324551del	GRCh38
NC_000013.10:g.23898689_23898690del , CM000675.1:g.23898689_23898690del	GRCh37
NC_000013.9:g.22796689_22796690del	NCBI36
NG_008759.1:g.148630_148631del , LRG_207:g.148630_148631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-12435_2186-12434del (SACS)	ENSP00000508399.1:n.2186-12435_2186-12434del
ENST00000683210.1:c.2185+29235_2185+29236del (SACS)	ENSP00000506739.1:n.2185+29235_2185+29236del
ENST00000684325.1:c.2186-2876_2186-2875del (SACS)	ENSP00000508121.1:n.2186-2876_2186-2875del
ENST00000684497.1:c.2186-1906_2186-1905del (SACS)	ENSP00000507057.1:n.2186-1906_2186-1905del
ENST00000218867.4:c.*9_*10del (SGCG) MANE Select	ENSP00000218867.3:n.*9_*10del
ENST00000218867.3:c.*9_*10del (SGCG)	ENSP00000218867.3:n.*9_*10del
NM_000231.2:c.*9_*10del , LRG_207t1:c.*9_*10del (SGCG)	NP_000222.1:n.*9_*10del
XM_005266505.2:c.*9_*10del (SGCG)	XP_005266562.1:n.*9_*10del
XM_006719861.2:c.*9_*10del (SGCG)	XP_006719924.1:n.*9_*10del
XM_006719861.3:c.*9_*10del (SGCG)	XP_006719924.1:n.*9_*10del
XM_024449397.1:c.*9_*10del (SGCG)	XP_024305165.1:n.*9_*10del
NM_000231.3:c.*9_*10del (SGCG) MANE Select	NP_000222.2:n.*9_*10del
NM_001378244.1:c.*9_*10del (SGCG)	NP_001365173.1:n.*9_*10del
NM_001378245.1:c.*9_*10del (SGCG)	NP_001365174.1:n.*9_*10del
NM_001378246.1:c.*9_*10del (SGCG)	NP_001365175.1:n.*9_*10del