Canonical Allele Identifier: CA6909797

Gene: SACS SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23320673C>A , CM000675.2:g.23320673C>A	GRCh38
NC_000013.10:g.23894812C>A , CM000675.1:g.23894812C>A	GRCh37
NC_000013.9:g.22792812C>A	NCBI36
NG_008759.1:g.144753C>A , LRG_207:g.144753C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000231.3:c.615C>A (SGCG) MANE Select	NP_000222.2:p.Ala205=
ENST00000218867.4:c.615C>A (SGCG) MANE Select	ENSP00000218867.3:p.Ala205=
NM_000231.2:c.615C>A , LRG_207t1:c.615C>A (SGCG)	NP_000222.1:p.Ala205=
NM_001378244.1:c.669C>A (SGCG)	NP_001365173.1:p.Ala223=
NM_001378245.1:c.615C>A (SGCG)	NP_001365174.1:p.Ala205=
NM_001378246.1:c.615C>A (SGCG)	NP_001365175.1:p.Ala205=
ENST00000218867.3:c.615C>A (SGCG)	ENSP00000218867.3:p.Ala205=
ENST00000682775.1:c.2186-8558G>T (SACS)	ENSP00000508399.1:n.2186-8558G>T
ENST00000683210.1:c.2186-31430G>T (SACS)	ENSP00000506739.1:n.2186-31430G>T
ENST00000684325.1:c.*104+893G>T (SACS)	ENSP00000508121.1:n.*104+893G>T
XM_005266505.2:c.615C>A (SGCG)	XP_005266562.1:p.Ala205=
XM_006719861.2:c.669C>A (SGCG)	XP_006719924.1:p.Ala223=
XM_006719861.3:c.669C>A (SGCG)	XP_006719924.1:p.Ala223=
XM_024449397.1:c.615C>A (SGCG)	XP_024305165.1:p.Ala205=
XR_001749787.1:n.1181+893G>T