Canonical Allele Identifier: CA563937671
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1383430588

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156594963del , CM000667.2:g.156594963del GRCh38
NC_000005.9:g.156021973del , CM000667.1:g.156021973del GRCh37
NC_000005.8:g.155954551del NCBI36
NG_008693.2:g.729620del , LRG_205:g.729620del

Transcript Alleles

HGVS Amino-acid Change
ENST00000337851.9:c.414del MANE Select ENSP00000338343.4:p.Lys138AsnfsTer4
ENST00000337851.8:c.414del ENSP00000338343.4:p.Lys138AsnfsTer4
ENST00000435422.7:c.411del ENSP00000403003.2:p.Lys137AsnfsTer4
ENST00000517913.5:c.414del ENSP00000429378.1:p.Lys138AsnfsTer4
NM_000337.5:c.414del , LRG_205t1:c.414del NP_000328.2:p.Lys138AsnfsTer4
NM_001128209.1:c.411del NP_001121681.1:p.Lys137AsnfsTer4
NM_172244.2:c.414del NP_758447.1:p.Lys138AsnfsTer4
XM_005265966.3:c.414del XP_005266023.1:p.Lys138AsnfsTer4
XM_005265967.1:c.414del XP_005266024.1:p.Lys138AsnfsTer4
XM_006714911.2:c.414del XP_006714974.1:p.Lys138AsnfsTer4
XM_011534621.1:c.411del XP_011532923.1:p.Lys137AsnfsTer4
XM_005265966.5:c.414del XP_005266023.1:p.Lys138AsnfsTer4
XM_005265967.2:c.414del XP_005266024.1:p.Lys138AsnfsTer4
XM_011534621.2:c.411del XP_011532923.1:p.Lys137AsnfsTer4
XM_017009723.2:c.414del XP_016865212.1:p.Lys138AsnfsTer4
XM_017009724.1:c.414del XP_016865213.1:p.Lys138AsnfsTer4
NM_001128209.2:c.411del NP_001121681.1:p.Lys137AsnfsTer4
NM_172244.3:c.414del NP_758447.1:p.Lys138AsnfsTer4
NM_000337.6:c.414del MANE Select NP_000328.2:p.Lys138AsnfsTer4