Canonical Allele Identifier: CA1445208522

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156757C= , CM000666.2:g.25156757C=	GRCh38
NC_000004.11:g.25158379C= , CM000666.1:g.25158379C=	GRCh37
NC_000004.10:g.24767477C=	NCBI36
NG_028222.1:g.8826G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+99G= MANE Select	ENSP00000371535.2:n.388+99G=
ENST00000680581.1:c.388+99G=	ENSP00000506483.1:n.388+99G=
ENST00000680824.1:n.1604+99G=
ENST00000681071.1:n.680+99G=
ENST00000681166.1:n.1435+99G=
ENST00000681341.1:n.1529+99G=
ENST00000681640.1:n.482+99G=
ENST00000681948.1:c.643+99G=	ENSP00000505991.1:n.643+99G=
ENST00000358971.7:c.*186+99G=	ENSP00000351857.3:n.*186+99G=
ENST00000382103.6:c.388+99G=	ENSP00000371535.2:n.388+99G=
ENST00000514585.5:c.*89+99G=	ENSP00000421880.1:n.*89+99G=
NM_016955.3:c.388+99G=	NP_058651.3:n.388+99G=
XM_005248168.2:c.151+99G=	XP_005248225.1:n.151+99G=
XM_006713965.2:c.208+99G=	XP_006714028.1:n.208+99G=
XM_011513846.1:c.385+99G=	XP_011512148.1:n.385+99G=
XM_011513847.1:c.355+99G=	XP_011512149.1:n.355+99G=
XM_011513848.1:c.208+99G=	XP_011512150.1:n.208+99G=
XM_011513846.2:c.385+99G=	XP_011512148.1:n.385+99G=
XM_011513847.2:c.355+99G=	XP_011512149.1:n.355+99G=
XM_017008277.1:c.643+99G=	XP_016863766.1:n.643+99G=
XM_017008278.1:c.-36+99G=	XP_016863767.1:n.-36+99G=
NM_016955.4:c.388+99G= MANE Select	NP_058651.3:n.388+99G=