Canonical Allele Identifier: CA1445204340
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25120762T= , CM000666.2:g.25120762T= GRCh38
NC_000004.11:g.25122384T= , CM000666.1:g.25122384T= GRCh37
NC_000004.10:g.24731482T= NCBI36
NG_028222.1:g.44821A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.*3169A= MANE Select ENSP00000371535.2:n.*3169A=
ENST00000680581.1:c.*3549A= ENSP00000506483.1:n.*3549A=
ENST00000680824.1:n.5891A=
ENST00000681071.1:n.4967A=
ENST00000681341.1:n.5722A=
ENST00000681374.1:n.4031A=
ENST00000681948.1:c.*3169A= ENSP00000505991.1:n.*3169A=
ENST00000382103.6:c.*3169A= ENSP00000371535.2:n.*3169A=
NM_016955.3:c.*3169A= NP_058651.3:n.*3169A=
XM_005248168.2:c.*3169A= XP_005248225.1:n.*3169A=
XM_006713965.2:c.*3169A= XP_006714028.1:n.*3169A=
XM_011513846.1:c.*3169A= XP_011512148.1:n.*3169A=
XM_011513847.1:c.*3169A= XP_011512149.1:n.*3169A=
XM_011513848.1:c.*3169A= XP_011512150.1:n.*3169A=
XM_011513846.2:c.*3169A= XP_011512148.1:n.*3169A=
XM_011513847.2:c.*3169A= XP_011512149.1:n.*3169A=
XM_017008277.1:c.*3169A= XP_016863766.1:n.*3169A=
XM_017008278.1:c.*3169A= XP_016863767.1:n.*3169A=
NM_016955.4:c.*3169A= MANE Select NP_058651.3:n.*3169A=