Canonical Allele Identifier: CA1445223228

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144792C= , CM000666.2:g.25144792C=	GRCh38
NC_000004.11:g.25146414C= , CM000666.1:g.25146414C=	GRCh37
NC_000004.10:g.24755512C=	NCBI36
NG_028222.1:g.20791G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1008G= MANE Select	ENSP00000371535.2:p.Lys336=
ENST00000680581.1:c.1008G=	ENSP00000506483.1:p.Lys336=
ENST00000680824.1:n.2224G=
ENST00000681071.1:n.1300G=
ENST00000681341.1:n.2149G=
ENST00000681948.1:c.1263G=	ENSP00000505991.1:p.Lys421=
ENST00000358971.7:c.*806G=	ENSP00000351857.3:n.*806G=
ENST00000382103.6:c.1008G=	ENSP00000371535.2:p.Lys336=
ENST00000503150.1:c.290G=
ENST00000505513.1:n.308G=
ENST00000514585.5:c.*709G=	ENSP00000421880.1:n.*709G=
NM_016955.3:c.1008G=	NP_058651.3:p.Lys336=
XM_005248168.2:c.771G=	XP_005248225.1:p.Lys257=
XM_006713965.2:c.828G=	XP_006714028.1:p.Lys276=
XM_011513846.1:c.1005G=	XP_011512148.1:p.Lys335=
XM_011513847.1:c.975G=	XP_011512149.1:p.Lys325=
XM_011513848.1:c.828G=	XP_011512150.1:p.Lys276=
XM_011513846.2:c.1005G=	XP_011512148.1:p.Lys335=
XM_011513847.2:c.975G=	XP_011512149.1:p.Lys325=
XM_017008277.1:c.1263G=	XP_016863766.1:p.Lys421=
XM_017008278.1:c.585G=	XP_016863767.1:p.Lys195=
NM_016955.4:c.1008G= MANE Select	NP_058651.3:p.Lys336=