Canonical Allele Identifier: CA356542534
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156856C>G , CM000666.2:g.25156856C>G GRCh38
NC_000004.11:g.25158478C>G , CM000666.1:g.25158478C>G GRCh37
NC_000004.10:g.24767576C>G NCBI36
NG_028222.1:g.8727G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382103.7:c.388G>C MANE Select ENSP00000371535.2:p.Gly130Arg
ENST00000680581.1:c.388G>C ENSP00000506483.1:p.Gly130Arg
ENST00000680824.1:n.1604G>C
ENST00000681071.1:n.680G>C
ENST00000681166.1:n.1435G>C
ENST00000681341.1:n.1529G>C
ENST00000681640.1:n.482G>C
ENST00000681948.1:c.643G>C ENSP00000505991.1:p.Gly215Arg
ENST00000358971.7:c.*186G>C ENSP00000351857.3:n.*186G>C
ENST00000382103.6:c.388G>C ENSP00000371535.2:p.Gly130Arg
ENST00000514585.5:c.*89G>C ENSP00000421880.1:n.*89G>C
NM_016955.3:c.388G>C NP_058651.3:p.Gly130Arg
XM_005248168.2:c.151G>C XP_005248225.1:p.Gly51Arg
XM_006713965.2:c.208G>C XP_006714028.1:p.Gly70Arg
XM_011513846.1:c.385G>C XP_011512148.1:p.Gly129Arg
XM_011513847.1:c.355G>C XP_011512149.1:p.Gly119Arg
XM_011513848.1:c.208G>C XP_011512150.1:p.Gly70Arg
XM_011513846.2:c.385G>C XP_011512148.1:p.Gly129Arg
XM_011513847.2:c.355G>C XP_011512149.1:p.Gly119Arg
XM_017008277.1:c.643G>C XP_016863766.1:p.Gly215Arg
XM_017008278.1:c.-36G>C XP_016863767.1:n.-36G>C
NM_016955.4:c.388G>C MANE Select NP_058651.3:p.Gly130Arg