Canonical Allele Identifier: CA356542550
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.380A>C MANE Select ENSP00000371535.2:p.Lys127Thr
ENST00000680581.1:c.380A>C ENSP00000506483.1:p.Lys127Thr
ENST00000680824.1:n.1596A>C
ENST00000681071.1:n.672A>C
ENST00000681166.1:n.1427A>C
ENST00000681341.1:n.1521A>C
ENST00000681640.1:n.474A>C
ENST00000681948.1:c.635A>C ENSP00000505991.1:p.Lys212Thr
ENST00000358971.7:c.*178A>C ENSP00000351857.3:n.*178A>C
ENST00000382103.6:c.380A>C ENSP00000371535.2:p.Lys127Thr
ENST00000514585.5:c.*81A>C ENSP00000421880.1:n.*81A>C
NM_016955.3:c.380A>C NP_058651.3:p.Lys127Thr
XM_005248168.2:c.143A>C XP_005248225.1:p.Lys48Thr
XM_006713965.2:c.200A>C XP_006714028.1:p.Lys67Thr
XM_011513846.1:c.377A>C XP_011512148.1:p.Lys126Thr
XM_011513847.1:c.347A>C XP_011512149.1:p.Lys116Thr
XM_011513848.1:c.200A>C XP_011512150.1:p.Lys67Thr
XM_011513846.2:c.377A>C XP_011512148.1:p.Lys126Thr
XM_011513847.2:c.347A>C XP_011512149.1:p.Lys116Thr
XM_017008277.1:c.635A>C XP_016863766.1:p.Lys212Thr
XM_017008278.1:c.-44A>C XP_016863767.1:n.-44A>C
NM_016955.4:c.380A>C MANE Select NP_058651.3:p.Lys127Thr