Canonical Allele Identifier: CA356536714
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144795C>G , CM000666.2:g.25144795C>G GRCh38
NC_000004.11:g.25146417C>G , CM000666.1:g.25146417C>G GRCh37
NC_000004.10:g.24755515C>G NCBI36
NG_028222.1:g.20788G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1005G>C MANE Select ENSP00000371535.2:p.Lys335Asn
ENST00000680581.1:c.1005G>C ENSP00000506483.1:p.Lys335Asn
ENST00000680824.1:n.2221G>C
ENST00000681071.1:n.1297G>C
ENST00000681341.1:n.2146G>C
ENST00000681948.1:c.1260G>C ENSP00000505991.1:p.Lys420Asn
ENST00000358971.7:c.*803G>C ENSP00000351857.3:n.*803G>C
ENST00000382103.6:c.1005G>C ENSP00000371535.2:p.Lys335Asn
ENST00000503150.1:c.287G>C
ENST00000505513.1:n.305G>C
ENST00000514585.5:c.*706G>C ENSP00000421880.1:n.*706G>C
NM_016955.3:c.1005G>C NP_058651.3:p.Lys335Asn
XM_005248168.2:c.768G>C XP_005248225.1:p.Lys256Asn
XM_006713965.2:c.825G>C XP_006714028.1:p.Lys275Asn
XM_011513846.1:c.1002G>C XP_011512148.1:p.Lys334Asn
XM_011513847.1:c.972G>C XP_011512149.1:p.Lys324Asn
XM_011513848.1:c.825G>C XP_011512150.1:p.Lys275Asn
XM_011513846.2:c.1002G>C XP_011512148.1:p.Lys334Asn
XM_011513847.2:c.972G>C XP_011512149.1:p.Lys324Asn
XM_017008277.1:c.1260G>C XP_016863766.1:p.Lys420Asn
XM_017008278.1:c.582G>C XP_016863767.1:p.Lys194Asn
NM_016955.4:c.1005G>C MANE Select NP_058651.3:p.Lys335Asn