Canonical Allele Identifier: CA356542608

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158513G>A (hg19) ; chr4:g.25156891G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156891G>A , CM000666.2:g.25156891G>A	GRCh38
NC_000004.11:g.25158513G>A , CM000666.1:g.25158513G>A	GRCh37
NC_000004.10:g.24767611G>A	NCBI36
NG_028222.1:g.8692C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.353C>T MANE Select	ENSP00000371535.2:p.Thr118Ile
ENST00000680581.1:c.353C>T	ENSP00000506483.1:p.Thr118Ile
ENST00000680824.1:n.1569C>T
ENST00000681071.1:n.645C>T
ENST00000681166.1:n.1400C>T
ENST00000681341.1:n.1494C>T
ENST00000681640.1:n.447C>T
ENST00000681948.1:c.608C>T	ENSP00000505991.1:p.Thr203Ile
ENST00000358971.7:c.*151C>T	ENSP00000351857.3:n.*151C>T
ENST00000382103.6:c.353C>T	ENSP00000371535.2:p.Thr118Ile
ENST00000514585.5:c.*54C>T	ENSP00000421880.1:n.*54C>T
NM_016955.3:c.353C>T	NP_058651.3:p.Thr118Ile
XM_005248168.2:c.116C>T	XP_005248225.1:p.Thr39Ile
XM_006713965.2:c.173C>T	XP_006714028.1:p.Thr58Ile
XM_011513846.1:c.350C>T	XP_011512148.1:p.Thr117Ile
XM_011513847.1:c.320C>T	XP_011512149.1:p.Thr107Ile
XM_011513848.1:c.173C>T	XP_011512150.1:p.Thr58Ile
XM_011513846.2:c.350C>T	XP_011512148.1:p.Thr117Ile
XM_011513847.2:c.320C>T	XP_011512149.1:p.Thr107Ile
XM_017008277.1:c.608C>T	XP_016863766.1:p.Thr203Ile
XM_017008278.1:c.-71C>T	XP_016863767.1:n.-71C>T
NM_016955.4:c.353C>T MANE Select	NP_058651.3:p.Thr118Ile