Canonical Allele Identifier: CA1445208705

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156871T= , CM000666.2:g.25156871T=	GRCh38
NC_000004.11:g.25158493T= , CM000666.1:g.25158493T=	GRCh37
NC_000004.10:g.24767591T=	NCBI36
NG_028222.1:g.8712A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.373A= MANE Select	ENSP00000371535.2:p.Ile125=
ENST00000680581.1:c.373A=	ENSP00000506483.1:p.Ile125=
ENST00000680824.1:n.1589A=
ENST00000681071.1:n.665A=
ENST00000681166.1:n.1420A=
ENST00000681341.1:n.1514A=
ENST00000681640.1:n.467A=
ENST00000681948.1:c.628A=	ENSP00000505991.1:p.Ile210=
ENST00000358971.7:c.*171A=	ENSP00000351857.3:n.*171A=
ENST00000382103.6:c.373A=	ENSP00000371535.2:p.Ile125=
ENST00000514585.5:c.*74A=	ENSP00000421880.1:n.*74A=
NM_016955.3:c.373A=	NP_058651.3:p.Ile125=
XM_005248168.2:c.136A=	XP_005248225.1:p.Ile46=
XM_006713965.2:c.193A=	XP_006714028.1:p.Ile65=
XM_011513846.1:c.370A=	XP_011512148.1:p.Ile124=
XM_011513847.1:c.340A=	XP_011512149.1:p.Ile114=
XM_011513848.1:c.193A=	XP_011512150.1:p.Ile65=
XM_011513846.2:c.370A=	XP_011512148.1:p.Ile124=
XM_011513847.2:c.340A=	XP_011512149.1:p.Ile114=
XM_017008277.1:c.628A=	XP_016863766.1:p.Ile210=
XM_017008278.1:c.-51A=	XP_016863767.1:n.-51A=
NM_016955.4:c.373A= MANE Select	NP_058651.3:p.Ile125=