Canonical Allele Identifier: CA1445208735

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156886A= , CM000666.2:g.25156886A=	GRCh38
NC_000004.11:g.25158508A= , CM000666.1:g.25158508A=	GRCh37
NC_000004.10:g.24767606A=	NCBI36
NG_028222.1:g.8697T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.358T= MANE Select	ENSP00000371535.2:p.Ser120=
ENST00000680581.1:c.358T=	ENSP00000506483.1:p.Ser120=
ENST00000680824.1:n.1574T=
ENST00000681071.1:n.650T=
ENST00000681166.1:n.1405T=
ENST00000681341.1:n.1499T=
ENST00000681640.1:n.452T=
ENST00000681948.1:c.613T=	ENSP00000505991.1:p.Ser205=
ENST00000358971.7:c.*156T=	ENSP00000351857.3:n.*156T=
ENST00000382103.6:c.358T=	ENSP00000371535.2:p.Ser120=
ENST00000514585.5:c.*59T=	ENSP00000421880.1:n.*59T=
NM_016955.3:c.358T=	NP_058651.3:p.Ser120=
XM_005248168.2:c.121T=	XP_005248225.1:p.Ser41=
XM_006713965.2:c.178T=	XP_006714028.1:p.Ser60=
XM_011513846.1:c.355T=	XP_011512148.1:p.Ser119=
XM_011513847.1:c.325T=	XP_011512149.1:p.Ser109=
XM_011513848.1:c.178T=	XP_011512150.1:p.Ser60=
XM_011513846.2:c.355T=	XP_011512148.1:p.Ser119=
XM_011513847.2:c.325T=	XP_011512149.1:p.Ser109=
XM_017008277.1:c.613T=	XP_016863766.1:p.Ser205=
XM_017008278.1:c.-66T=	XP_016863767.1:n.-66T=
NM_016955.4:c.358T= MANE Select	NP_058651.3:p.Ser120=