Canonical Allele Identifier: CA2670197275
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156860del , CM000666.2:g.25156860del GRCh38
NC_000004.11:g.25158482del , CM000666.1:g.25158482del GRCh37
NC_000004.10:g.24767580del NCBI36
NG_028222.1:g.8724del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.385del MANE Select ENSP00000371535.2:p.Ala129LeufsTer6
ENST00000680581.1:c.385del ENSP00000506483.1:p.Ala129LeufsTer6
ENST00000680824.1:n.1601del
ENST00000681071.1:n.677del
ENST00000681166.1:n.1432del
ENST00000681341.1:n.1526del
ENST00000681640.1:n.479del
ENST00000681948.1:c.640del ENSP00000505991.1:p.Ala214LeufsTer6
ENST00000358971.7:c.*183del ENSP00000351857.3:n.*183del
ENST00000382103.6:c.385del ENSP00000371535.2:p.Ala129LeufsTer6
ENST00000514585.5:c.*86del ENSP00000421880.1:n.*86del
NM_016955.3:c.385del NP_058651.3:p.Ala129LeufsTer6
XM_005248168.2:c.148del XP_005248225.1:p.Ala50LeufsTer6
XM_006713965.2:c.205del XP_006714028.1:p.Ala69LeufsTer6
XM_011513846.1:c.382del XP_011512148.1:p.Ala128LeufsTer6
XM_011513847.1:c.352del XP_011512149.1:p.Ala118LeufsTer6
XM_011513848.1:c.205del XP_011512150.1:p.Ala69LeufsTer6
XM_011513846.2:c.382del XP_011512148.1:p.Ala128LeufsTer6
XM_011513847.2:c.352del XP_011512149.1:p.Ala118LeufsTer6
XM_017008277.1:c.640del XP_016863766.1:p.Ala214LeufsTer6
XM_017008278.1:c.-39del XP_016863767.1:n.-39del
NM_016955.4:c.385del MANE Select NP_058651.3:p.Ala129LeufsTer6