Canonical Allele Identifier: CA2676178102
Gene: SGCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508701del , CM000667.2:g.156508701del GRCh38
NC_000005.9:g.155935711del , CM000667.1:g.155935711del GRCh37
NC_000005.8:g.155868289del NCBI36
NG_008693.2:g.643358del , LRG_205:g.643358del

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.293del MANE Select ENSP00000338343.4:p.Pro98GlnfsTer15
ENST00000337851.8:c.293del ENSP00000338343.4:p.Pro98GlnfsTer15
ENST00000435422.7:c.290del ENSP00000403003.2:p.Pro97GlnfsTer15
ENST00000517913.5:c.293del ENSP00000429378.1:p.Pro98GlnfsTer15
ENST00000524347.2:c.*157del ENSP00000430794.1:n.*157del
NM_000337.5:c.293del , LRG_205t1:c.293del NP_000328.2:p.Pro98GlnfsTer15
NM_001128209.1:c.290del NP_001121681.1:p.Pro97GlnfsTer15
NM_172244.2:c.293del NP_758447.1:p.Pro98GlnfsTer15
XM_005265966.3:c.293del XP_005266023.1:p.Pro98GlnfsTer15
XM_005265967.1:c.293del XP_005266024.1:p.Pro98GlnfsTer15
XM_006714911.2:c.293del XP_006714974.1:p.Pro98GlnfsTer15
XM_011534621.1:c.290del XP_011532923.1:p.Pro97GlnfsTer15
XM_005265966.5:c.293del XP_005266023.1:p.Pro98GlnfsTer15
XM_005265967.2:c.293del XP_005266024.1:p.Pro98GlnfsTer15
XM_011534621.2:c.290del XP_011532923.1:p.Pro97GlnfsTer15
XM_017009723.2:c.293del XP_016865212.1:p.Pro98GlnfsTer15
XM_017009724.1:c.293del XP_016865213.1:p.Pro98GlnfsTer15
NM_001128209.2:c.290del NP_001121681.1:p.Pro97GlnfsTer15
NM_172244.3:c.293del NP_758447.1:p.Pro98GlnfsTer15
NM_000337.6:c.293del MANE Select NP_000328.2:p.Pro98GlnfsTer15