Canonical Allele Identifier: CA1445208710

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156872G= , CM000666.2:g.25156872G=	GRCh38
NC_000004.11:g.25158494G= , CM000666.1:g.25158494G=	GRCh37
NC_000004.10:g.24767592G=	NCBI36
NG_028222.1:g.8711C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.372C= MANE Select	ENSP00000371535.2:p.Asp124=
ENST00000680581.1:c.372C=	ENSP00000506483.1:p.Asp124=
ENST00000680824.1:n.1588C=
ENST00000681071.1:n.664C=
ENST00000681166.1:n.1419C=
ENST00000681341.1:n.1513C=
ENST00000681640.1:n.466C=
ENST00000681948.1:c.627C=	ENSP00000505991.1:p.Asp209=
ENST00000358971.7:c.*170C=	ENSP00000351857.3:n.*170C=
ENST00000382103.6:c.372C=	ENSP00000371535.2:p.Asp124=
ENST00000514585.5:c.*73C=	ENSP00000421880.1:n.*73C=
NM_016955.3:c.372C=	NP_058651.3:p.Asp124=
XM_005248168.2:c.135C=	XP_005248225.1:p.Asp45=
XM_006713965.2:c.192C=	XP_006714028.1:p.Asp64=
XM_011513846.1:c.369C=	XP_011512148.1:p.Asp123=
XM_011513847.1:c.339C=	XP_011512149.1:p.Asp113=
XM_011513848.1:c.192C=	XP_011512150.1:p.Asp64=
XM_011513846.2:c.369C=	XP_011512148.1:p.Asp123=
XM_011513847.2:c.339C=	XP_011512149.1:p.Asp113=
XM_017008277.1:c.627C=	XP_016863766.1:p.Asp209=
XM_017008278.1:c.-52C=	XP_016863767.1:n.-52C=
NM_016955.4:c.372C= MANE Select	NP_058651.3:p.Asp124=