Canonical Allele Identifier: CA356536646
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144781T>C , CM000666.2:g.25144781T>C GRCh38
NC_000004.11:g.25146403T>C , CM000666.1:g.25146403T>C GRCh37
NC_000004.10:g.24755501T>C NCBI36
NG_028222.1:g.20802A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1019A>G MANE Select ENSP00000371535.2:p.Glu340Gly
ENST00000680581.1:c.1019A>G ENSP00000506483.1:p.Glu340Gly
ENST00000680824.1:n.2235A>G
ENST00000681071.1:n.1311A>G
ENST00000681341.1:n.2160A>G
ENST00000681948.1:c.1274A>G ENSP00000505991.1:p.Glu425Gly
ENST00000358971.7:c.*817A>G ENSP00000351857.3:n.*817A>G
ENST00000382103.6:c.1019A>G ENSP00000371535.2:p.Glu340Gly
ENST00000503150.1:c.301A>G
ENST00000505513.1:n.319A>G
ENST00000514585.5:c.*720A>G ENSP00000421880.1:n.*720A>G
NM_016955.3:c.1019A>G NP_058651.3:p.Glu340Gly
XM_005248168.2:c.782A>G XP_005248225.1:p.Glu261Gly
XM_006713965.2:c.839A>G XP_006714028.1:p.Glu280Gly
XM_011513846.1:c.1016A>G XP_011512148.1:p.Glu339Gly
XM_011513847.1:c.986A>G XP_011512149.1:p.Glu329Gly
XM_011513848.1:c.839A>G XP_011512150.1:p.Glu280Gly
XM_011513846.2:c.1016A>G XP_011512148.1:p.Glu339Gly
XM_011513847.2:c.986A>G XP_011512149.1:p.Glu329Gly
XM_017008277.1:c.1274A>G XP_016863766.1:p.Glu425Gly
XM_017008278.1:c.596A>G XP_016863767.1:p.Glu199Gly
NM_016955.4:c.1019A>G MANE Select NP_058651.3:p.Glu340Gly