Canonical Allele Identifier: CA2575388451
Gene: SGCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23250580_23250582del , CM000675.2:g.23250580_23250582del GRCh38
NC_000013.10:g.23824719_23824721del , CM000675.1:g.23824719_23824721del GRCh37
NC_000013.9:g.22722719_22722721del NCBI36
NG_008759.1:g.74660_74662del , LRG_207:g.74660_74662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218867.4:c.298-50_298-48del MANE Select ENSP00000218867.3:n.298-50_298-48del
ENST00000218867.3:c.298-50_298-48del ENSP00000218867.3:n.298-50_298-48del
NM_000231.2:c.298-50_298-48del , LRG_207t1:c.298-50_298-48del NP_000222.1:n.298-50_298-48del
XM_005266505.2:c.298-50_298-48del XP_005266562.1:n.298-50_298-48del
XM_006719861.2:c.352-50_352-48del XP_006719924.1:n.352-50_352-48del
XM_006719861.3:c.352-50_352-48del XP_006719924.1:n.352-50_352-48del
XM_024449397.1:c.298-50_298-48del XP_024305165.1:n.298-50_298-48del
NM_000231.3:c.298-50_298-48del MANE Select NP_000222.2:n.298-50_298-48del
NM_001378244.1:c.352-50_352-48del NP_001365173.1:n.352-50_352-48del
NM_001378245.1:c.298-50_298-48del NP_001365174.1:n.298-50_298-48del
NM_001378246.1:c.298-50_298-48del NP_001365175.1:n.298-50_298-48del