Canonical Allele Identifier: CA1445208642

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156843A= , CM000666.2:g.25156843A=	GRCh38
NC_000004.11:g.25158465A= , CM000666.1:g.25158465A=	GRCh37
NC_000004.10:g.24767563A=	NCBI36
NG_028222.1:g.8740T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+13T= MANE Select	ENSP00000371535.2:n.388+13T=
ENST00000680581.1:c.388+13T=	ENSP00000506483.1:n.388+13T=
ENST00000680824.1:n.1604+13T=
ENST00000681071.1:n.680+13T=
ENST00000681166.1:n.1435+13T=
ENST00000681341.1:n.1529+13T=
ENST00000681640.1:n.482+13T=
ENST00000681948.1:c.643+13T=	ENSP00000505991.1:n.643+13T=
ENST00000358971.7:c.*186+13T=	ENSP00000351857.3:n.*186+13T=
ENST00000382103.6:c.388+13T=	ENSP00000371535.2:n.388+13T=
ENST00000514585.5:c.*89+13T=	ENSP00000421880.1:n.*89+13T=
NM_016955.3:c.388+13T=	NP_058651.3:n.388+13T=
XM_005248168.2:c.151+13T=	XP_005248225.1:n.151+13T=
XM_006713965.2:c.208+13T=	XP_006714028.1:n.208+13T=
XM_011513846.1:c.385+13T=	XP_011512148.1:n.385+13T=
XM_011513847.1:c.355+13T=	XP_011512149.1:n.355+13T=
XM_011513848.1:c.208+13T=	XP_011512150.1:n.208+13T=
XM_011513846.2:c.385+13T=	XP_011512148.1:n.385+13T=
XM_011513847.2:c.355+13T=	XP_011512149.1:n.355+13T=
XM_017008277.1:c.643+13T=	XP_016863766.1:n.643+13T=
XM_017008278.1:c.-36+13T=	XP_016863767.1:n.-36+13T=
NM_016955.4:c.388+13T= MANE Select	NP_058651.3:n.388+13T=