Canonical Allele Identifier: CA1445208681

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156862G= , CM000666.2:g.25156862G=	GRCh38
NC_000004.11:g.25158484G= , CM000666.1:g.25158484G=	GRCh37
NC_000004.10:g.24767582G=	NCBI36
NG_028222.1:g.8721C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.382C= MANE Select	ENSP00000371535.2:p.Leu128=
ENST00000680581.1:c.382C=	ENSP00000506483.1:p.Leu128=
ENST00000680824.1:n.1598C=
ENST00000681071.1:n.674C=
ENST00000681166.1:n.1429C=
ENST00000681341.1:n.1523C=
ENST00000681640.1:n.476C=
ENST00000681948.1:c.637C=	ENSP00000505991.1:p.Leu213=
ENST00000358971.7:c.*180C=	ENSP00000351857.3:n.*180C=
ENST00000382103.6:c.382C=	ENSP00000371535.2:p.Leu128=
ENST00000514585.5:c.*83C=	ENSP00000421880.1:n.*83C=
NM_016955.3:c.382C=	NP_058651.3:p.Leu128=
XM_005248168.2:c.145C=	XP_005248225.1:p.Leu49=
XM_006713965.2:c.202C=	XP_006714028.1:p.Leu68=
XM_011513846.1:c.379C=	XP_011512148.1:p.Leu127=
XM_011513847.1:c.349C=	XP_011512149.1:p.Leu117=
XM_011513848.1:c.202C=	XP_011512150.1:p.Leu68=
XM_011513846.2:c.379C=	XP_011512148.1:p.Leu127=
XM_011513847.2:c.349C=	XP_011512149.1:p.Leu117=
XM_017008277.1:c.637C=	XP_016863766.1:p.Leu213=
XM_017008278.1:c.-42C=	XP_016863767.1:n.-42C=
NM_016955.4:c.382C= MANE Select	NP_058651.3:p.Leu128=