Canonical Allele Identifier: CA1445208745

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156898T= , CM000666.2:g.25156898T=	GRCh38
NC_000004.11:g.25158520T= , CM000666.1:g.25158520T=	GRCh37
NC_000004.10:g.24767618T=	NCBI36
NG_028222.1:g.8685A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.346A= MANE Select	ENSP00000371535.2:p.Lys116=
ENST00000680581.1:c.346A=	ENSP00000506483.1:p.Lys116=
ENST00000680824.1:n.1562A=
ENST00000681071.1:n.638A=
ENST00000681166.1:n.1393A=
ENST00000681341.1:n.1487A=
ENST00000681640.1:n.440A=
ENST00000681948.1:c.601A=	ENSP00000505991.1:p.Lys201=
ENST00000358971.7:c.*144A=	ENSP00000351857.3:n.*144A=
ENST00000382103.6:c.346A=	ENSP00000371535.2:p.Lys116=
ENST00000514585.5:c.*47A=	ENSP00000421880.1:n.*47A=
NM_016955.3:c.346A=	NP_058651.3:p.Lys116=
XM_005248168.2:c.109A=	XP_005248225.1:p.Lys37=
XM_006713965.2:c.166A=	XP_006714028.1:p.Lys56=
XM_011513846.1:c.343A=	XP_011512148.1:p.Lys115=
XM_011513847.1:c.313A=	XP_011512149.1:p.Lys105=
XM_011513848.1:c.166A=	XP_011512150.1:p.Lys56=
XM_011513846.2:c.343A=	XP_011512148.1:p.Lys115=
XM_011513847.2:c.313A=	XP_011512149.1:p.Lys105=
XM_017008277.1:c.601A=	XP_016863766.1:p.Lys201=
XM_017008278.1:c.-78A=	XP_016863767.1:n.-78A=
NM_016955.4:c.346A= MANE Select	NP_058651.3:p.Lys116=