Canonical Allele Identifier: CA2739277463
Gene: SGCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23203783del , CM000675.2:g.23203783del GRCh38
NC_000013.10:g.23777922del , CM000675.1:g.23777922del GRCh37
NC_000013.9:g.22675922del NCBI36
NG_008759.1:g.27863del , LRG_207:g.27863del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218867.4:c.89del MANE Select ENSP00000218867.3:p.Gly30AlafsTer20
ENST00000218867.3:c.89del ENSP00000218867.3:p.Gly30AlafsTer20
NM_000231.2:c.89del , LRG_207t1:c.89del NP_000222.1:p.Gly30AlafsTer20
XM_005266505.2:c.89del XP_005266562.1:p.Gly30AlafsTer20
XM_006719861.2:c.143del XP_006719924.1:p.Gly48AlafsTer20
XM_006719861.3:c.143del XP_006719924.1:p.Gly48AlafsTer20
XM_024449397.1:c.89del XP_024305165.1:p.Gly30AlafsTer20
NM_000231.3:c.89del MANE Select NP_000222.2:p.Gly30AlafsTer20
NM_001378244.1:c.143del NP_001365173.1:p.Gly48AlafsTer20
NM_001378245.1:c.89del NP_001365174.1:p.Gly30AlafsTer20
NM_001378246.1:c.89del NP_001365175.1:p.Gly30AlafsTer20