Canonical Allele Identifier: CA438732700

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158488T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156866T>A , CM000666.2:g.25156866T>A	GRCh38
NC_000004.11:g.25158488T>A , CM000666.1:g.25158488T>A	GRCh37
NC_000004.10:g.24767586T>A	NCBI36
NG_028222.1:g.8717A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.378A>T MANE Select	ENSP00000371535.2:p.Ile126=
ENST00000680581.1:c.378A>T	ENSP00000506483.1:p.Ile126=
ENST00000680824.1:n.1594A>T
ENST00000681071.1:n.670A>T
ENST00000681166.1:n.1425A>T
ENST00000681341.1:n.1519A>T
ENST00000681640.1:n.472A>T
ENST00000681948.1:c.633A>T	ENSP00000505991.1:p.Ile211=
ENST00000358971.7:c.*176A>T	ENSP00000351857.3:n.*176A>T
ENST00000382103.6:c.378A>T	ENSP00000371535.2:p.Ile126=
ENST00000514585.5:c.*79A>T	ENSP00000421880.1:n.*79A>T
NM_016955.3:c.378A>T	NP_058651.3:p.Ile126=
XM_005248168.2:c.141A>T	XP_005248225.1:p.Ile47=
XM_006713965.2:c.198A>T	XP_006714028.1:p.Ile66=
XM_011513846.1:c.375A>T	XP_011512148.1:p.Ile125=
XM_011513847.1:c.345A>T	XP_011512149.1:p.Ile115=
XM_011513848.1:c.198A>T	XP_011512150.1:p.Ile66=
XM_011513846.2:c.375A>T	XP_011512148.1:p.Ile125=
XM_011513847.2:c.345A>T	XP_011512149.1:p.Ile115=
XM_017008277.1:c.633A>T	XP_016863766.1:p.Ile211=
XM_017008278.1:c.-46A>T	XP_016863767.1:n.-46A>T
NM_016955.4:c.378A>T MANE Select	NP_058651.3:p.Ile126=