Canonical Allele Identifier: CA356542601

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25158510T>G (hg19) ; chr4:g.25156888T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156888T>G , CM000666.2:g.25156888T>G	GRCh38
NC_000004.11:g.25158510T>G , CM000666.1:g.25158510T>G	GRCh37
NC_000004.10:g.24767608T>G	NCBI36
NG_028222.1:g.8695A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.356A>C MANE Select	ENSP00000371535.2:p.Asn119Thr
ENST00000680581.1:c.356A>C	ENSP00000506483.1:p.Asn119Thr
ENST00000680824.1:n.1572A>C
ENST00000681071.1:n.648A>C
ENST00000681166.1:n.1403A>C
ENST00000681341.1:n.1497A>C
ENST00000681640.1:n.450A>C
ENST00000681948.1:c.611A>C	ENSP00000505991.1:p.Asn204Thr
ENST00000358971.7:c.*154A>C	ENSP00000351857.3:n.*154A>C
ENST00000382103.6:c.356A>C	ENSP00000371535.2:p.Asn119Thr
ENST00000514585.5:c.*57A>C	ENSP00000421880.1:n.*57A>C
NM_016955.3:c.356A>C	NP_058651.3:p.Asn119Thr
XM_005248168.2:c.119A>C	XP_005248225.1:p.Asn40Thr
XM_006713965.2:c.176A>C	XP_006714028.1:p.Asn59Thr
XM_011513846.1:c.353A>C	XP_011512148.1:p.Asn118Thr
XM_011513847.1:c.323A>C	XP_011512149.1:p.Asn108Thr
XM_011513848.1:c.176A>C	XP_011512150.1:p.Asn59Thr
XM_011513846.2:c.353A>C	XP_011512148.1:p.Asn118Thr
XM_011513847.2:c.323A>C	XP_011512149.1:p.Asn108Thr
XM_017008277.1:c.611A>C	XP_016863766.1:p.Asn204Thr
XM_017008278.1:c.-68A>C	XP_016863767.1:n.-68A>C
NM_016955.4:c.356A>C MANE Select	NP_058651.3:p.Asn119Thr