Canonical Allele Identifier: CA356542551
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.380A>G MANE Select ENSP00000371535.2:p.Lys127Arg
ENST00000680581.1:c.380A>G ENSP00000506483.1:p.Lys127Arg
ENST00000680824.1:n.1596A>G
ENST00000681071.1:n.672A>G
ENST00000681166.1:n.1427A>G
ENST00000681341.1:n.1521A>G
ENST00000681640.1:n.474A>G
ENST00000681948.1:c.635A>G ENSP00000505991.1:p.Lys212Arg
ENST00000358971.7:c.*178A>G ENSP00000351857.3:n.*178A>G
ENST00000382103.6:c.380A>G ENSP00000371535.2:p.Lys127Arg
ENST00000514585.5:c.*81A>G ENSP00000421880.1:n.*81A>G
NM_016955.3:c.380A>G NP_058651.3:p.Lys127Arg
XM_005248168.2:c.143A>G XP_005248225.1:p.Lys48Arg
XM_006713965.2:c.200A>G XP_006714028.1:p.Lys67Arg
XM_011513846.1:c.377A>G XP_011512148.1:p.Lys126Arg
XM_011513847.1:c.347A>G XP_011512149.1:p.Lys116Arg
XM_011513848.1:c.200A>G XP_011512150.1:p.Lys67Arg
XM_011513846.2:c.377A>G XP_011512148.1:p.Lys126Arg
XM_011513847.2:c.347A>G XP_011512149.1:p.Lys116Arg
XM_017008277.1:c.635A>G XP_016863766.1:p.Lys212Arg
XM_017008278.1:c.-44A>G XP_016863767.1:n.-44A>G
NM_016955.4:c.380A>G MANE Select NP_058651.3:p.Lys127Arg