Canonical Allele Identifier: CA2078576247

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23181109A= , CM000675.2:g.23181109A=	GRCh38
NC_000013.10:g.23755248A= , CM000675.1:g.23755248A=	GRCh37
NC_000013.9:g.22653248A=	NCBI36
NG_008759.1:g.5189A= , LRG_207:g.5189A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.-1+34A= MANE Select	ENSP00000218867.3:n.-1+34A=
ENST00000218867.3:c.-1+34A=	ENSP00000218867.3:n.-1+34A=
NM_000231.2:c.-1+34A= , LRG_207t1:c.-1+34A=	NP_000222.1:n.-1+34A=
XM_005266505.2:c.-152+34A=	XP_005266562.1:n.-152+34A=
XM_006719861.2:c.54+20463A=	XP_006719924.1:n.54+20463A=
XM_006719861.3:c.54+20463A=	XP_006719924.1:n.54+20463A=
XM_024449397.1:c.-152+126A=	XP_024305165.1:n.-152+126A=
NM_000231.3:c.-1+34A= MANE Select	NP_000222.2:n.-1+34A=
NM_001378244.1:c.54+20463A=	NP_001365173.1:n.54+20463A=
NM_001378245.1:c.-152+126A=	NP_001365174.1:n.-152+126A=
NM_001378246.1:c.-152+34A=	NP_001365175.1:n.-152+34A=