Canonical Allele Identifier: CA356536699
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144792C>A , CM000666.2:g.25144792C>A GRCh38
NC_000004.11:g.25146414C>A , CM000666.1:g.25146414C>A GRCh37
NC_000004.10:g.24755512C>A NCBI36
NG_028222.1:g.20791G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1008G>T MANE Select ENSP00000371535.2:p.Lys336Asn
ENST00000680581.1:c.1008G>T ENSP00000506483.1:p.Lys336Asn
ENST00000680824.1:n.2224G>T
ENST00000681071.1:n.1300G>T
ENST00000681341.1:n.2149G>T
ENST00000681948.1:c.1263G>T ENSP00000505991.1:p.Lys421Asn
ENST00000358971.7:c.*806G>T ENSP00000351857.3:n.*806G>T
ENST00000382103.6:c.1008G>T ENSP00000371535.2:p.Lys336Asn
ENST00000503150.1:c.290G>T
ENST00000505513.1:n.308G>T
ENST00000514585.5:c.*709G>T ENSP00000421880.1:n.*709G>T
NM_016955.3:c.1008G>T NP_058651.3:p.Lys336Asn
XM_005248168.2:c.771G>T XP_005248225.1:p.Lys257Asn
XM_006713965.2:c.828G>T XP_006714028.1:p.Lys276Asn
XM_011513846.1:c.1005G>T XP_011512148.1:p.Lys335Asn
XM_011513847.1:c.975G>T XP_011512149.1:p.Lys325Asn
XM_011513848.1:c.828G>T XP_011512150.1:p.Lys276Asn
XM_011513846.2:c.1005G>T XP_011512148.1:p.Lys335Asn
XM_011513847.2:c.975G>T XP_011512149.1:p.Lys325Asn
XM_017008277.1:c.1263G>T XP_016863766.1:p.Lys421Asn
XM_017008278.1:c.585G>T XP_016863767.1:p.Lys195Asn
NM_016955.4:c.1008G>T MANE Select NP_058651.3:p.Lys336Asn