Canonical Allele Identifier: CA356536705
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144793T>C , CM000666.2:g.25144793T>C GRCh38
NC_000004.11:g.25146415T>C , CM000666.1:g.25146415T>C GRCh37
NC_000004.10:g.24755513T>C NCBI36
NG_028222.1:g.20790A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1007A>G MANE Select ENSP00000371535.2:p.Lys336Arg
ENST00000680581.1:c.1007A>G ENSP00000506483.1:p.Lys336Arg
ENST00000680824.1:n.2223A>G
ENST00000681071.1:n.1299A>G
ENST00000681341.1:n.2148A>G
ENST00000681948.1:c.1262A>G ENSP00000505991.1:p.Lys421Arg
ENST00000358971.7:c.*805A>G ENSP00000351857.3:n.*805A>G
ENST00000382103.6:c.1007A>G ENSP00000371535.2:p.Lys336Arg
ENST00000503150.1:c.289A>G
ENST00000505513.1:n.307A>G
ENST00000514585.5:c.*708A>G ENSP00000421880.1:n.*708A>G
NM_016955.3:c.1007A>G NP_058651.3:p.Lys336Arg
XM_005248168.2:c.770A>G XP_005248225.1:p.Lys257Arg
XM_006713965.2:c.827A>G XP_006714028.1:p.Lys276Arg
XM_011513846.1:c.1004A>G XP_011512148.1:p.Lys335Arg
XM_011513847.1:c.974A>G XP_011512149.1:p.Lys325Arg
XM_011513848.1:c.827A>G XP_011512150.1:p.Lys276Arg
XM_011513846.2:c.1004A>G XP_011512148.1:p.Lys335Arg
XM_011513847.2:c.974A>G XP_011512149.1:p.Lys325Arg
XM_017008277.1:c.1262A>G XP_016863766.1:p.Lys421Arg
XM_017008278.1:c.584A>G XP_016863767.1:p.Lys195Arg
NM_016955.4:c.1007A>G MANE Select NP_058651.3:p.Lys336Arg