Canonical Allele Identifier: CA1445223276

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144856G= , CM000666.2:g.25144856G=	GRCh38
NC_000004.11:g.25146478G= , CM000666.1:g.25146478G=	GRCh37
NC_000004.10:g.24755576G=	NCBI36
NG_028222.1:g.20727C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.944C= MANE Select	ENSP00000371535.2:p.Ser315=
ENST00000680581.1:c.944C=	ENSP00000506483.1:p.Ser315=
ENST00000680824.1:n.2160C=
ENST00000681071.1:n.1236C=
ENST00000681341.1:n.2085C=
ENST00000681948.1:c.1199C=	ENSP00000505991.1:p.Ser400=
ENST00000358971.7:c.*742C=	ENSP00000351857.3:n.*742C=
ENST00000382103.6:c.944C=	ENSP00000371535.2:p.Ser315=
ENST00000503150.1:c.226C=
ENST00000505513.1:n.244C=
ENST00000514585.5:c.*645C=	ENSP00000421880.1:n.*645C=
NM_016955.3:c.944C=	NP_058651.3:p.Ser315=
XM_005248168.2:c.707C=	XP_005248225.1:p.Ser236=
XM_006713965.2:c.764C=	XP_006714028.1:p.Ser255=
XM_011513846.1:c.941C=	XP_011512148.1:p.Ser314=
XM_011513847.1:c.911C=	XP_011512149.1:p.Ser304=
XM_011513848.1:c.764C=	XP_011512150.1:p.Ser255=
XM_011513846.2:c.941C=	XP_011512148.1:p.Ser314=
XM_011513847.2:c.911C=	XP_011512149.1:p.Ser304=
XM_017008277.1:c.1199C=	XP_016863766.1:p.Ser400=
XM_017008278.1:c.521C=	XP_016863767.1:p.Ser174=
NM_016955.4:c.944C= MANE Select	NP_058651.3:p.Ser315=