Canonical Allele Identifier: CA1445206854

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25123971T= , CM000666.2:g.25123971T=	GRCh38
NC_000004.11:g.25125593T= , CM000666.1:g.25125593T=	GRCh37
NC_000004.10:g.24734691T=	NCBI36
NG_028222.1:g.41612A=

Transcript Alleles

HGVS	Amino-acid Change
NM_016955.4:c.1466A= MANE Select	NP_058651.3:p.Asp489=
ENST00000382103.7:c.1466A= MANE Select	ENSP00000371535.2:p.Asp489=
NM_016955.3:c.1466A=	NP_058651.3:p.Asp489=
ENST00000358971.7:c.*1264A=	ENSP00000351857.3:n.*1264A=
ENST00000382103.6:c.1466A=	ENSP00000371535.2:p.Asp489=
ENST00000514585.5:c.*1167A=	ENSP00000421880.1:n.*1167A=
ENST00000680581.1:c.*340A=	ENSP00000506483.1:n.*340A=
ENST00000680824.1:n.2682A=
ENST00000681071.1:n.1758A=
ENST00000681341.1:n.2513A=
ENST00000681374.1:n.822A=
ENST00000681948.1:c.1721A=	ENSP00000505991.1:p.Asp574=
XM_005248168.2:c.1229A=	XP_005248225.1:p.Asp410=
XM_006713965.2:c.1286A=	XP_006714028.1:p.Asp429=
XM_011513846.1:c.1463A=	XP_011512148.1:p.Asp488=
XM_011513846.2:c.1463A=	XP_011512148.1:p.Asp488=
XM_011513847.1:c.1433A=	XP_011512149.1:p.Asp478=
XM_011513847.2:c.1433A=	XP_011512149.1:p.Asp478=
XM_011513848.1:c.1286A=	XP_011512150.1:p.Asp429=
XM_017008277.1:c.1721A=	XP_016863766.1:p.Asp574=
XM_017008278.1:c.1043A=	XP_016863767.1:p.Asp348=