Canonical Allele Identifier: CA1445223230

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144795C= , CM000666.2:g.25144795C=	GRCh38
NC_000004.11:g.25146417C= , CM000666.1:g.25146417C=	GRCh37
NC_000004.10:g.24755515C=	NCBI36
NG_028222.1:g.20788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1005G= MANE Select	ENSP00000371535.2:p.Lys335=
ENST00000680581.1:c.1005G=	ENSP00000506483.1:p.Lys335=
ENST00000680824.1:n.2221G=
ENST00000681071.1:n.1297G=
ENST00000681341.1:n.2146G=
ENST00000681948.1:c.1260G=	ENSP00000505991.1:p.Lys420=
ENST00000358971.7:c.*803G=	ENSP00000351857.3:n.*803G=
ENST00000382103.6:c.1005G=	ENSP00000371535.2:p.Lys335=
ENST00000503150.1:c.287G=
ENST00000505513.1:n.305G=
ENST00000514585.5:c.*706G=	ENSP00000421880.1:n.*706G=
NM_016955.3:c.1005G=	NP_058651.3:p.Lys335=
XM_005248168.2:c.768G=	XP_005248225.1:p.Lys256=
XM_006713965.2:c.825G=	XP_006714028.1:p.Lys275=
XM_011513846.1:c.1002G=	XP_011512148.1:p.Lys334=
XM_011513847.1:c.972G=	XP_011512149.1:p.Lys324=
XM_011513848.1:c.825G=	XP_011512150.1:p.Lys275=
XM_011513846.2:c.1002G=	XP_011512148.1:p.Lys334=
XM_011513847.2:c.972G=	XP_011512149.1:p.Lys324=
XM_017008277.1:c.1260G=	XP_016863766.1:p.Lys420=
XM_017008278.1:c.582G=	XP_016863767.1:p.Lys194=
NM_016955.4:c.1005G= MANE Select	NP_058651.3:p.Lys335=