Canonical Allele Identifier: CA1445208684
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156865T= , CM000666.2:g.25156865T= GRCh38
NC_000004.11:g.25158487T= , CM000666.1:g.25158487T= GRCh37
NC_000004.10:g.24767585T= NCBI36
NG_028222.1:g.8718A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.379A= MANE Select ENSP00000371535.2:p.Lys127=
ENST00000680581.1:c.379A= ENSP00000506483.1:p.Lys127=
ENST00000680824.1:n.1595A=
ENST00000681071.1:n.671A=
ENST00000681166.1:n.1426A=
ENST00000681341.1:n.1520A=
ENST00000681640.1:n.473A=
ENST00000681948.1:c.634A= ENSP00000505991.1:p.Lys212=
ENST00000358971.7:c.*177A= ENSP00000351857.3:n.*177A=
ENST00000382103.6:c.379A= ENSP00000371535.2:p.Lys127=
ENST00000514585.5:c.*80A= ENSP00000421880.1:n.*80A=
NM_016955.3:c.379A= NP_058651.3:p.Lys127=
XM_005248168.2:c.142A= XP_005248225.1:p.Lys48=
XM_006713965.2:c.199A= XP_006714028.1:p.Lys67=
XM_011513846.1:c.376A= XP_011512148.1:p.Lys126=
XM_011513847.1:c.346A= XP_011512149.1:p.Lys116=
XM_011513848.1:c.199A= XP_011512150.1:p.Lys67=
XM_011513846.2:c.376A= XP_011512148.1:p.Lys126=
XM_011513847.2:c.346A= XP_011512149.1:p.Lys116=
XM_017008277.1:c.634A= XP_016863766.1:p.Lys212=
XM_017008278.1:c.-45A= XP_016863767.1:n.-45A=
NM_016955.4:c.379A= MANE Select NP_058651.3:p.Lys127=