Canonical Allele Identifier: CA438732756

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158563A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156941A>T , CM000666.2:g.25156941A>T	GRCh38
NC_000004.11:g.25158563A>T , CM000666.1:g.25158563A>T	GRCh37
NC_000004.10:g.24767661A>T	NCBI36
NG_028222.1:g.8642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.303T>A MANE Select	ENSP00000371535.2:p.Ile101=
ENST00000680581.1:c.303T>A	ENSP00000506483.1:p.Ile101=
ENST00000680824.1:n.1519T>A
ENST00000681071.1:n.595T>A
ENST00000681166.1:n.1350T>A
ENST00000681341.1:n.1444T>A
ENST00000681640.1:n.397T>A
ENST00000681948.1:c.558T>A	ENSP00000505991.1:p.Ile186=
ENST00000358971.7:c.*101T>A	ENSP00000351857.3:n.*101T>A
ENST00000382103.6:c.303T>A	ENSP00000371535.2:p.Ile101=
ENST00000514585.5:c.*4T>A	ENSP00000421880.1:n.*4T>A
NM_016955.3:c.303T>A	NP_058651.3:p.Ile101=
XM_005248168.2:c.66T>A	XP_005248225.1:p.Ile22=
XM_006713965.2:c.123T>A	XP_006714028.1:p.Ile41=
XM_011513846.1:c.300T>A	XP_011512148.1:p.Ile100=
XM_011513847.1:c.270T>A	XP_011512149.1:p.Ile90=
XM_011513848.1:c.123T>A	XP_011512150.1:p.Ile41=
XM_011513846.2:c.300T>A	XP_011512148.1:p.Ile100=
XM_011513847.2:c.270T>A	XP_011512149.1:p.Ile90=
XM_017008277.1:c.558T>A	XP_016863766.1:p.Ile186=
XM_017008278.1:c.-121T>A	XP_016863767.1:n.-121T>A
NM_016955.4:c.303T>A MANE Select	NP_058651.3:p.Ile101=