Canonical Allele Identifier: CA1445208737

Gene: SEPSECS

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.356A= MANE Select	ENSP00000371535.2:p.Asn119=
ENST00000680581.1:c.356A=	ENSP00000506483.1:p.Asn119=
ENST00000680824.1:n.1572A=
ENST00000681071.1:n.648A=
ENST00000681166.1:n.1403A=
ENST00000681341.1:n.1497A=
ENST00000681640.1:n.450A=
ENST00000681948.1:c.611A=	ENSP00000505991.1:p.Asn204=
ENST00000358971.7:c.*154A=	ENSP00000351857.3:n.*154A=
ENST00000382103.6:c.356A=	ENSP00000371535.2:p.Asn119=
ENST00000514585.5:c.*57A=	ENSP00000421880.1:n.*57A=
NM_016955.3:c.356A=	NP_058651.3:p.Asn119=
XM_005248168.2:c.119A=	XP_005248225.1:p.Asn40=
XM_006713965.2:c.176A=	XP_006714028.1:p.Asn59=
XM_011513846.1:c.353A=	XP_011512148.1:p.Asn118=
XM_011513847.1:c.323A=	XP_011512149.1:p.Asn108=
XM_011513848.1:c.176A=	XP_011512150.1:p.Asn59=
XM_011513846.2:c.353A=	XP_011512148.1:p.Asn118=
XM_011513847.2:c.323A=	XP_011512149.1:p.Asn108=
XM_017008277.1:c.611A=	XP_016863766.1:p.Asn204=
XM_017008278.1:c.-68A=	XP_016863767.1:n.-68A=
NM_016955.4:c.356A= MANE Select	NP_058651.3:p.Asn119=