Canonical Allele Identifier: CA1445227781

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25152049C= , CM000666.2:g.25152049C=	GRCh38
NC_000004.11:g.25153671C= , CM000666.1:g.25153671C=	GRCh37
NC_000004.10:g.24762769C=	NCBI36
NG_028222.1:g.13534G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016955.4:c.715G= MANE Select	NP_058651.3:p.Ala239=
ENST00000382103.7:c.715G= MANE Select	ENSP00000371535.2:p.Ala239=
NM_016955.3:c.715G=	NP_058651.3:p.Ala239=
ENST00000358971.7:c.*513G=	ENSP00000351857.3:n.*513G=
ENST00000382103.6:c.715G=	ENSP00000371535.2:p.Ala239=
ENST00000503150.1:c.216+2949G=
ENST00000505513.1:n.234+2949G=
ENST00000514585.5:c.*416G=	ENSP00000421880.1:n.*416G=
ENST00000680581.1:c.715G=	ENSP00000506483.1:p.Ala239=
ENST00000680824.1:n.1931G=
ENST00000681071.1:n.1007G=
ENST00000681341.1:n.1856G=
ENST00000681948.1:c.970G=	ENSP00000505991.1:p.Ala324=
XM_005248168.2:c.478G=	XP_005248225.1:p.Ala160=
XM_006713965.2:c.535G=	XP_006714028.1:p.Ala179=
XM_011513846.1:c.712G=	XP_011512148.1:p.Ala238=
XM_011513846.2:c.712G=	XP_011512148.1:p.Ala238=
XM_011513847.1:c.682G=	XP_011512149.1:p.Ala228=
XM_011513847.2:c.682G=	XP_011512149.1:p.Ala228=
XM_011513848.1:c.535G=	XP_011512150.1:p.Ala179=
XM_017008277.1:c.970G=	XP_016863766.1:p.Ala324=
XM_017008278.1:c.292G=	XP_016863767.1:p.Ala98=