Canonical Allele Identifier: CA1445208825

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156950G= , CM000666.2:g.25156950G=	GRCh38
NC_000004.11:g.25158572G= , CM000666.1:g.25158572G=	GRCh37
NC_000004.10:g.24767670G=	NCBI36
NG_028222.1:g.8633C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.294C= MANE Select	ENSP00000371535.2:p.Ser98=
ENST00000680581.1:c.294C=	ENSP00000506483.1:p.Ser98=
ENST00000680824.1:n.1510C=
ENST00000681071.1:n.586C=
ENST00000681166.1:n.1341C=
ENST00000681341.1:n.1435C=
ENST00000681640.1:n.388C=
ENST00000681948.1:c.549C=	ENSP00000505991.1:p.Ser183=
ENST00000358971.7:c.*92C=	ENSP00000351857.3:n.*92C=
ENST00000382103.6:c.294C=	ENSP00000371535.2:p.Ser98=
ENST00000514585.5:c.139C=	ENSP00000421880.1:p.Arg47=
NM_016955.3:c.294C=	NP_058651.3:p.Ser98=
XM_005248168.2:c.57C=	XP_005248225.1:p.Ser19=
XM_006713965.2:c.114C=	XP_006714028.1:p.Ser38=
XM_011513846.1:c.291C=	XP_011512148.1:p.Ser97=
XM_011513847.1:c.261C=	XP_011512149.1:p.Ser87=
XM_011513848.1:c.114C=	XP_011512150.1:p.Ser38=
XM_011513846.2:c.291C=	XP_011512148.1:p.Ser97=
XM_011513847.2:c.261C=	XP_011512149.1:p.Ser87=
XM_017008277.1:c.549C=	XP_016863766.1:p.Ser183=
XM_017008278.1:c.-130C=	XP_016863767.1:n.-130C=
NM_016955.4:c.294C= MANE Select	NP_058651.3:p.Ser98=