Canonical Allele Identifier: CA2078576199

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23180998A= , CM000675.2:g.23180998A=	GRCh38
NC_000013.10:g.23755137A= , CM000675.1:g.23755137A=	GRCh37
NC_000013.9:g.22653137A=	NCBI36
NG_008759.1:g.5078A= , LRG_207:g.5078A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.-78A= MANE Select	ENSP00000218867.3:n.-78A=
ENST00000218867.3:c.-78A=	ENSP00000218867.3:n.-78A=
NM_000231.2:c.-78A= , LRG_207t1:c.-78A=	NP_000222.1:n.-78A=
XM_005266505.2:c.-229A=	XP_005266562.1:n.-229A=
XM_006719861.2:c.54+20352A=	XP_006719924.1:n.54+20352A=
XM_006719861.3:c.54+20352A=	XP_006719924.1:n.54+20352A=
XM_024449397.1:c.-152+15A=	XP_024305165.1:n.-152+15A=
NM_000231.3:c.-78A= MANE Select	NP_000222.2:n.-78A=
NM_001378244.1:c.54+20352A=	NP_001365173.1:n.54+20352A=
NM_001378245.1:c.-152+15A=	NP_001365174.1:n.-152+15A=
NM_001378246.1:c.-229A=	NP_001365175.1:n.-229A=