Canonical Allele Identifier: CA2078590998

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23250696G= , CM000675.2:g.23250696G=	GRCh38
NC_000013.10:g.23824835G= , CM000675.1:g.23824835G=	GRCh37
NC_000013.9:g.22722835G=	NCBI36
NG_008759.1:g.74776G= , LRG_207:g.74776G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.364G= MANE Select	ENSP00000218867.3:p.Val122=
ENST00000218867.3:c.364G=	ENSP00000218867.3:p.Val122=
NM_000231.2:c.364G= , LRG_207t1:c.364G=	NP_000222.1:p.Val122=
XM_005266505.2:c.364G=	XP_005266562.1:p.Val122=
XM_006719861.2:c.418G=	XP_006719924.1:p.Val140=
XM_006719861.3:c.418G=	XP_006719924.1:p.Val140=
XM_024449397.1:c.364G=	XP_024305165.1:p.Val122=
NM_000231.3:c.364G= MANE Select	NP_000222.2:p.Val122=
NM_001378244.1:c.418G=	NP_001365173.1:p.Val140=
NM_001378245.1:c.364G=	NP_001365174.1:p.Val122=
NM_001378246.1:c.364G=	NP_001365175.1:p.Val122=