Canonical Allele Identifier: CA2078621206

Gene: SACS SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23324450A= , CM000675.2:g.23324450A=	GRCh38
NC_000013.10:g.23898589A= , CM000675.1:g.23898589A=	GRCh37
NC_000013.9:g.22796589A=	NCBI36
NG_008759.1:g.148530A= , LRG_207:g.148530A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-12335T= (SACS)	ENSP00000508399.1:n.2186-12335T=
ENST00000683210.1:c.2185+29335T= (SACS)	ENSP00000506739.1:n.2185+29335T=
ENST00000684325.1:c.2186-2776T= (SACS)	ENSP00000508121.1:n.2186-2776T=
ENST00000684497.1:c.2186-1806T= (SACS)	ENSP00000507057.1:n.2186-1806T=
ENST00000218867.4:c.785A= (SGCG) MANE Select	ENSP00000218867.3:p.Tyr262=
ENST00000218867.3:c.785A= (SGCG)	ENSP00000218867.3:p.Tyr262=
NM_000231.2:c.785A= , LRG_207t1:c.785A= (SGCG)	NP_000222.1:p.Tyr262=
XM_005266505.2:c.785A= (SGCG)	XP_005266562.1:p.Tyr262=
XM_006719861.2:c.839A= (SGCG)	XP_006719924.1:p.Tyr280=
XM_006719861.3:c.839A= (SGCG)	XP_006719924.1:p.Tyr280=
XM_024449397.1:c.785A= (SGCG)	XP_024305165.1:p.Tyr262=
NM_000231.3:c.785A= (SGCG) MANE Select	NP_000222.2:p.Tyr262=
NM_001378244.1:c.839A= (SGCG)	NP_001365173.1:p.Tyr280=
NM_001378245.1:c.785A= (SGCG)	NP_001365174.1:p.Tyr262=
NM_001378246.1:c.785A= (SGCG)	NP_001365175.1:p.Tyr262=