Canonical Allele Identifier: CA1445223244

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144804A= , CM000666.2:g.25144804A=	GRCh38
NC_000004.11:g.25146426A= , CM000666.1:g.25146426A=	GRCh37
NC_000004.10:g.24755524A=	NCBI36
NG_028222.1:g.20779T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.996T= MANE Select	ENSP00000371535.2:p.Asn332=
ENST00000680581.1:c.996T=	ENSP00000506483.1:p.Asn332=
ENST00000680824.1:n.2212T=
ENST00000681071.1:n.1288T=
ENST00000681341.1:n.2137T=
ENST00000681948.1:c.1251T=	ENSP00000505991.1:p.Asn417=
ENST00000358971.7:c.*794T=	ENSP00000351857.3:n.*794T=
ENST00000382103.6:c.996T=	ENSP00000371535.2:p.Asn332=
ENST00000503150.1:c.278T=
ENST00000505513.1:n.296T=
ENST00000514585.5:c.*697T=	ENSP00000421880.1:n.*697T=
NM_016955.3:c.996T=	NP_058651.3:p.Asn332=
XM_005248168.2:c.759T=	XP_005248225.1:p.Asn253=
XM_006713965.2:c.816T=	XP_006714028.1:p.Asn272=
XM_011513846.1:c.993T=	XP_011512148.1:p.Asn331=
XM_011513847.1:c.963T=	XP_011512149.1:p.Asn321=
XM_011513848.1:c.816T=	XP_011512150.1:p.Asn272=
XM_011513846.2:c.993T=	XP_011512148.1:p.Asn331=
XM_011513847.2:c.963T=	XP_011512149.1:p.Asn321=
XM_017008277.1:c.1251T=	XP_016863766.1:p.Asn417=
XM_017008278.1:c.573T=	XP_016863767.1:p.Asn191=
NM_016955.4:c.996T= MANE Select	NP_058651.3:p.Asn332=