Canonical Allele Identifier: CA356542605

Gene: SEPSECS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.353C>A MANE Select	ENSP00000371535.2:p.Thr118Asn
ENST00000680581.1:c.353C>A	ENSP00000506483.1:p.Thr118Asn
ENST00000680824.1:n.1569C>A
ENST00000681071.1:n.645C>A
ENST00000681166.1:n.1400C>A
ENST00000681341.1:n.1494C>A
ENST00000681640.1:n.447C>A
ENST00000681948.1:c.608C>A	ENSP00000505991.1:p.Thr203Asn
ENST00000358971.7:c.*151C>A	ENSP00000351857.3:n.*151C>A
ENST00000382103.6:c.353C>A	ENSP00000371535.2:p.Thr118Asn
ENST00000514585.5:c.*54C>A	ENSP00000421880.1:n.*54C>A
NM_016955.3:c.353C>A	NP_058651.3:p.Thr118Asn
XM_005248168.2:c.116C>A	XP_005248225.1:p.Thr39Asn
XM_006713965.2:c.173C>A	XP_006714028.1:p.Thr58Asn
XM_011513846.1:c.350C>A	XP_011512148.1:p.Thr117Asn
XM_011513847.1:c.320C>A	XP_011512149.1:p.Thr107Asn
XM_011513848.1:c.173C>A	XP_011512150.1:p.Thr58Asn
XM_011513846.2:c.350C>A	XP_011512148.1:p.Thr117Asn
XM_011513847.2:c.320C>A	XP_011512149.1:p.Thr107Asn
XM_017008277.1:c.608C>A	XP_016863766.1:p.Thr203Asn
XM_017008278.1:c.-71C>A	XP_016863767.1:n.-71C>A
NM_016955.4:c.353C>A MANE Select	NP_058651.3:p.Thr118Asn