Canonical Allele Identifier: CA356542549
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156864T>A , CM000666.2:g.25156864T>A GRCh38
NC_000004.11:g.25158486T>A , CM000666.1:g.25158486T>A GRCh37
NC_000004.10:g.24767584T>A NCBI36
NG_028222.1:g.8719A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.380A>T MANE Select ENSP00000371535.2:p.Lys127Met
ENST00000680581.1:c.380A>T ENSP00000506483.1:p.Lys127Met
ENST00000680824.1:n.1596A>T
ENST00000681071.1:n.672A>T
ENST00000681166.1:n.1427A>T
ENST00000681341.1:n.1521A>T
ENST00000681640.1:n.474A>T
ENST00000681948.1:c.635A>T ENSP00000505991.1:p.Lys212Met
ENST00000358971.7:c.*178A>T ENSP00000351857.3:n.*178A>T
ENST00000382103.6:c.380A>T ENSP00000371535.2:p.Lys127Met
ENST00000514585.5:c.*81A>T ENSP00000421880.1:n.*81A>T
NM_016955.3:c.380A>T NP_058651.3:p.Lys127Met
XM_005248168.2:c.143A>T XP_005248225.1:p.Lys48Met
XM_006713965.2:c.200A>T XP_006714028.1:p.Lys67Met
XM_011513846.1:c.377A>T XP_011512148.1:p.Lys126Met
XM_011513847.1:c.347A>T XP_011512149.1:p.Lys116Met
XM_011513848.1:c.200A>T XP_011512150.1:p.Lys67Met
XM_011513846.2:c.377A>T XP_011512148.1:p.Lys126Met
XM_011513847.2:c.347A>T XP_011512149.1:p.Lys116Met
XM_017008277.1:c.635A>T XP_016863766.1:p.Lys212Met
XM_017008278.1:c.-44A>T XP_016863767.1:n.-44A>T
NM_016955.4:c.380A>T MANE Select NP_058651.3:p.Lys127Met