Canonical Allele Identifier: CA438732716

Gene: SEPSECS

Linked Data

• COSMIC: COSM389493
• MyVariant Identifiers: chr4:g.25158512G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156890G>A , CM000666.2:g.25156890G>A	GRCh38
NC_000004.11:g.25158512G>A , CM000666.1:g.25158512G>A	GRCh37
NC_000004.10:g.24767610G>A	NCBI36
NG_028222.1:g.8693C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.354C>T MANE Select	ENSP00000371535.2:p.Thr118=
ENST00000680581.1:c.354C>T	ENSP00000506483.1:p.Thr118=
ENST00000680824.1:n.1570C>T
ENST00000681071.1:n.646C>T
ENST00000681166.1:n.1401C>T
ENST00000681341.1:n.1495C>T
ENST00000681640.1:n.448C>T
ENST00000681948.1:c.609C>T	ENSP00000505991.1:p.Thr203=
ENST00000358971.7:c.*152C>T	ENSP00000351857.3:n.*152C>T
ENST00000382103.6:c.354C>T	ENSP00000371535.2:p.Thr118=
ENST00000514585.5:c.*55C>T	ENSP00000421880.1:n.*55C>T
NM_016955.3:c.354C>T	NP_058651.3:p.Thr118=
XM_005248168.2:c.117C>T	XP_005248225.1:p.Thr39=
XM_006713965.2:c.174C>T	XP_006714028.1:p.Thr58=
XM_011513846.1:c.351C>T	XP_011512148.1:p.Thr117=
XM_011513847.1:c.321C>T	XP_011512149.1:p.Thr107=
XM_011513848.1:c.174C>T	XP_011512150.1:p.Thr58=
XM_011513846.2:c.351C>T	XP_011512148.1:p.Thr117=
XM_011513847.2:c.321C>T	XP_011512149.1:p.Thr107=
XM_017008277.1:c.609C>T	XP_016863766.1:p.Thr203=
XM_017008278.1:c.-70C>T	XP_016863767.1:n.-70C>T
NM_016955.4:c.354C>T MANE Select	NP_058651.3:p.Thr118=