Canonical Allele Identifier: CA1445223212
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144774C= , CM000666.2:g.25144774C= GRCh38
NC_000004.11:g.25146396C= , CM000666.1:g.25146396C= GRCh37
NC_000004.10:g.24755494C= NCBI36
NG_028222.1:g.20809G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.1026G= MANE Select ENSP00000371535.2:p.Lys342=
ENST00000680581.1:c.1026G= ENSP00000506483.1:p.Lys342=
ENST00000680824.1:n.2242G=
ENST00000681071.1:n.1318G=
ENST00000681341.1:n.2167G=
ENST00000681948.1:c.1281G= ENSP00000505991.1:p.Lys427=
ENST00000358971.7:c.*824G= ENSP00000351857.3:n.*824G=
ENST00000382103.6:c.1026G= ENSP00000371535.2:p.Lys342=
ENST00000503150.1:c.308G=
ENST00000505513.1:n.326G=
ENST00000514585.5:c.*727G= ENSP00000421880.1:n.*727G=
NM_016955.3:c.1026G= NP_058651.3:p.Lys342=
XM_005248168.2:c.789G= XP_005248225.1:p.Lys263=
XM_006713965.2:c.846G= XP_006714028.1:p.Lys282=
XM_011513846.1:c.1023G= XP_011512148.1:p.Lys341=
XM_011513847.1:c.993G= XP_011512149.1:p.Lys331=
XM_011513848.1:c.846G= XP_011512150.1:p.Lys282=
XM_011513846.2:c.1023G= XP_011512148.1:p.Lys341=
XM_011513847.2:c.993G= XP_011512149.1:p.Lys331=
XM_017008277.1:c.1281G= XP_016863766.1:p.Lys427=
XM_017008278.1:c.603G= XP_016863767.1:p.Lys201=
NM_016955.4:c.1026G= MANE Select NP_058651.3:p.Lys342=