Canonical Allele Identifier: CA2739277462

Gene: SGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23203776del , CM000675.2:g.23203776del	GRCh38
NC_000013.10:g.23777915del , CM000675.1:g.23777915del	GRCh37
NC_000013.9:g.22675915del	NCBI36
NG_008759.1:g.27856del , LRG_207:g.27856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218867.4:c.82del MANE Select	ENSP00000218867.3:p.Ile28PhefsTer22
ENST00000218867.3:c.82del	ENSP00000218867.3:p.Ile28PhefsTer22
NM_000231.2:c.82del , LRG_207t1:c.82del	NP_000222.1:p.Ile28PhefsTer22
XM_005266505.2:c.82del	XP_005266562.1:p.Ile28PhefsTer22
XM_006719861.2:c.136del	XP_006719924.1:p.Ile46PhefsTer22
XM_006719861.3:c.136del	XP_006719924.1:p.Ile46PhefsTer22
XM_024449397.1:c.82del	XP_024305165.1:p.Ile28PhefsTer22
NM_000231.3:c.82del MANE Select	NP_000222.2:p.Ile28PhefsTer22
NM_001378244.1:c.136del	NP_001365173.1:p.Ile46PhefsTer22
NM_001378245.1:c.82del	NP_001365174.1:p.Ile28PhefsTer22
NM_001378246.1:c.82del	NP_001365175.1:p.Ile28PhefsTer22