Canonical Allele Identifier: CA2580086801
Community Standard Title: NM_000231.3(SGCG):c.369dup (p.Gly124ArgfsTer?)
Gene: SGCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23250701dup , CM000675.2:g.23250701dup GRCh38
NC_000013.10:g.23824840dup , CM000675.1:g.23824840dup GRCh37
NC_000013.9:g.22722840dup NCBI36
NG_008759.1:g.74781dup , LRG_207:g.74781dup

Transcript Alleles

HGVS Amino-acid Change
NM_000231.3:c.369dup MANE Select NP_000222.2:p.Gly124ArgfsTer?
ENST00000218867.4:c.369dup MANE Select ENSP00000218867.3:p.Gly124ArgfsTer?
NM_000231.2:c.369dup , LRG_207t1:c.369dup NP_000222.1:p.Gly124ArgfsTer?
NM_001378244.1:c.423dup NP_001365173.1:p.Gly142ArgfsTer?
NM_001378245.1:c.369dup NP_001365174.1:p.Gly124ArgfsTer?
NM_001378246.1:c.369dup NP_001365175.1:p.Gly124ArgfsTer?
ENST00000218867.3:c.369dup ENSP00000218867.3:p.Gly124ArgfsTer?
XM_005266505.2:c.369dup XP_005266562.1:p.Gly124ArgfsTer?
XM_006719861.2:c.423dup XP_006719924.1:p.Gly142ArgfsTer?
XM_006719861.3:c.423dup XP_006719924.1:p.Gly142ArgfsTer?
XM_024449397.1:c.369dup XP_024305165.1:p.Gly124ArgfsTer?