Canonical Allele Identifier: CA1445208721
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156877G= , CM000666.2:g.25156877G= GRCh38
NC_000004.11:g.25158499G= , CM000666.1:g.25158499G= GRCh37
NC_000004.10:g.24767597G= NCBI36
NG_028222.1:g.8706C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.367C= MANE Select ENSP00000371535.2:p.Leu123=
ENST00000680581.1:c.367C= ENSP00000506483.1:p.Leu123=
ENST00000680824.1:n.1583C=
ENST00000681071.1:n.659C=
ENST00000681166.1:n.1414C=
ENST00000681341.1:n.1508C=
ENST00000681640.1:n.461C=
ENST00000681948.1:c.622C= ENSP00000505991.1:p.Leu208=
ENST00000358971.7:c.*165C= ENSP00000351857.3:n.*165C=
ENST00000382103.6:c.367C= ENSP00000371535.2:p.Leu123=
ENST00000514585.5:c.*68C= ENSP00000421880.1:n.*68C=
NM_016955.3:c.367C= NP_058651.3:p.Leu123=
XM_005248168.2:c.130C= XP_005248225.1:p.Leu44=
XM_006713965.2:c.187C= XP_006714028.1:p.Leu63=
XM_011513846.1:c.364C= XP_011512148.1:p.Leu122=
XM_011513847.1:c.334C= XP_011512149.1:p.Leu112=
XM_011513848.1:c.187C= XP_011512150.1:p.Leu63=
XM_011513846.2:c.364C= XP_011512148.1:p.Leu122=
XM_011513847.2:c.334C= XP_011512149.1:p.Leu112=
XM_017008277.1:c.622C= XP_016863766.1:p.Leu208=
XM_017008278.1:c.-57C= XP_016863767.1:n.-57C=
NM_016955.4:c.367C= MANE Select NP_058651.3:p.Leu123=