Canonical Allele Identifier: CA356536726
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144797T>A , CM000666.2:g.25144797T>A GRCh38
NC_000004.11:g.25146419T>A , CM000666.1:g.25146419T>A GRCh37
NC_000004.10:g.24755517T>A NCBI36
NG_028222.1:g.20786A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1003A>T MANE Select ENSP00000371535.2:p.Lys335Ter
ENST00000680581.1:c.1003A>T ENSP00000506483.1:p.Lys335Ter
ENST00000680824.1:n.2219A>T
ENST00000681071.1:n.1295A>T
ENST00000681341.1:n.2144A>T
ENST00000681948.1:c.1258A>T ENSP00000505991.1:p.Lys420Ter
ENST00000358971.7:c.*801A>T ENSP00000351857.3:n.*801A>T
ENST00000382103.6:c.1003A>T ENSP00000371535.2:p.Lys335Ter
ENST00000503150.1:c.285A>T
ENST00000505513.1:n.303A>T
ENST00000514585.5:c.*704A>T ENSP00000421880.1:n.*704A>T
NM_016955.3:c.1003A>T NP_058651.3:p.Lys335Ter
XM_005248168.2:c.766A>T XP_005248225.1:p.Lys256Ter
XM_006713965.2:c.823A>T XP_006714028.1:p.Lys275Ter
XM_011513846.1:c.1000A>T XP_011512148.1:p.Lys334Ter
XM_011513847.1:c.970A>T XP_011512149.1:p.Lys324Ter
XM_011513848.1:c.823A>T XP_011512150.1:p.Lys275Ter
XM_011513846.2:c.1000A>T XP_011512148.1:p.Lys334Ter
XM_011513847.2:c.970A>T XP_011512149.1:p.Lys324Ter
XM_017008277.1:c.1258A>T XP_016863766.1:p.Lys420Ter
XM_017008278.1:c.580A>T XP_016863767.1:p.Lys194Ter
NM_016955.4:c.1003A>T MANE Select NP_058651.3:p.Lys335Ter