Canonical Allele Identifier: CA1445208697

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156868T= , CM000666.2:g.25156868T=	GRCh38
NC_000004.11:g.25158490T= , CM000666.1:g.25158490T=	GRCh37
NC_000004.10:g.24767588T=	NCBI36
NG_028222.1:g.8715A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.376A= MANE Select	ENSP00000371535.2:p.Ile126=
ENST00000680581.1:c.376A=	ENSP00000506483.1:p.Ile126=
ENST00000680824.1:n.1592A=
ENST00000681071.1:n.668A=
ENST00000681166.1:n.1423A=
ENST00000681341.1:n.1517A=
ENST00000681640.1:n.470A=
ENST00000681948.1:c.631A=	ENSP00000505991.1:p.Ile211=
ENST00000358971.7:c.*174A=	ENSP00000351857.3:n.*174A=
ENST00000382103.6:c.376A=	ENSP00000371535.2:p.Ile126=
ENST00000514585.5:c.*77A=	ENSP00000421880.1:n.*77A=
NM_016955.3:c.376A=	NP_058651.3:p.Ile126=
XM_005248168.2:c.139A=	XP_005248225.1:p.Ile47=
XM_006713965.2:c.196A=	XP_006714028.1:p.Ile66=
XM_011513846.1:c.373A=	XP_011512148.1:p.Ile125=
XM_011513847.1:c.343A=	XP_011512149.1:p.Ile115=
XM_011513848.1:c.196A=	XP_011512150.1:p.Ile66=
XM_011513846.2:c.373A=	XP_011512148.1:p.Ile125=
XM_011513847.2:c.343A=	XP_011512149.1:p.Ile115=
XM_017008277.1:c.631A=	XP_016863766.1:p.Ile211=
XM_017008278.1:c.-48A=	XP_016863767.1:n.-48A=
NM_016955.4:c.376A= MANE Select	NP_058651.3:p.Ile126=