Canonical Allele Identifier: CA1445223216

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144777T= , CM000666.2:g.25144777T=	GRCh38
NC_000004.11:g.25146399T= , CM000666.1:g.25146399T=	GRCh37
NC_000004.10:g.24755497T=	NCBI36
NG_028222.1:g.20806A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1023A= MANE Select	ENSP00000371535.2:p.Arg341=
ENST00000680581.1:c.1023A=	ENSP00000506483.1:p.Arg341=
ENST00000680824.1:n.2239A=
ENST00000681071.1:n.1315A=
ENST00000681341.1:n.2164A=
ENST00000681948.1:c.1278A=	ENSP00000505991.1:p.Arg426=
ENST00000358971.7:c.*821A=	ENSP00000351857.3:n.*821A=
ENST00000382103.6:c.1023A=	ENSP00000371535.2:p.Arg341=
ENST00000503150.1:c.305A=
ENST00000505513.1:n.323A=
ENST00000514585.5:c.*724A=	ENSP00000421880.1:n.*724A=
NM_016955.3:c.1023A=	NP_058651.3:p.Arg341=
XM_005248168.2:c.786A=	XP_005248225.1:p.Arg262=
XM_006713965.2:c.843A=	XP_006714028.1:p.Arg281=
XM_011513846.1:c.1020A=	XP_011512148.1:p.Arg340=
XM_011513847.1:c.990A=	XP_011512149.1:p.Arg330=
XM_011513848.1:c.843A=	XP_011512150.1:p.Arg281=
XM_011513846.2:c.1020A=	XP_011512148.1:p.Arg340=
XM_011513847.2:c.990A=	XP_011512149.1:p.Arg330=
XM_017008277.1:c.1278A=	XP_016863766.1:p.Arg426=
XM_017008278.1:c.600A=	XP_016863767.1:p.Arg200=
NM_016955.4:c.1023A= MANE Select	NP_058651.3:p.Arg341=