Canonical Allele Identifier: CA2838588096
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156964dup , CM000666.2:g.25156964dup GRCh38
NC_000004.11:g.25158586dup , CM000666.1:g.25158586dup GRCh37
NC_000004.10:g.24767684dup NCBI36
NG_028222.1:g.8620dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.281dup MANE Select ENSP00000371535.2:p.Ile95HisfsTer6
ENST00000680581.1:c.281dup ENSP00000506483.1:p.Ile95HisfsTer6
ENST00000680824.1:n.1497dup
ENST00000681071.1:n.573dup
ENST00000681166.1:n.1328dup
ENST00000681341.1:n.1422dup
ENST00000681640.1:n.375dup
ENST00000681948.1:c.536dup ENSP00000505991.1:p.Ile180HisfsTer6
ENST00000358971.7:c.*79dup ENSP00000351857.3:n.*79dup
ENST00000382103.6:c.281dup ENSP00000371535.2:p.Ile95HisfsTer6
ENST00000514585.5:c.126dup ENSP00000421880.1:p.His43AlafsTer21
NM_016955.3:c.281dup NP_058651.3:p.Ile95HisfsTer6
XM_005248168.2:c.44dup XP_005248225.1:p.Ile16HisfsTer6
XM_006713965.2:c.101dup XP_006714028.1:p.Ile35HisfsTer6
XM_011513846.1:c.278dup XP_011512148.1:p.Ile94HisfsTer6
XM_011513847.1:c.248dup XP_011512149.1:p.Ile84HisfsTer6
XM_011513848.1:c.101dup XP_011512150.1:p.Ile35HisfsTer6
XM_011513846.2:c.278dup XP_011512148.1:p.Ile94HisfsTer6
XM_011513847.2:c.248dup XP_011512149.1:p.Ile84HisfsTer6
XM_017008277.1:c.536dup XP_016863766.1:p.Ile180HisfsTer6
XM_017008278.1:c.-143dup XP_016863767.1:n.-143dup
NM_016955.4:c.281dup MANE Select NP_058651.3:p.Ile95HisfsTer6