Canonical Allele Identifier: CA1445208874

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156970T= , CM000666.2:g.25156970T=	GRCh38
NC_000004.11:g.25158592T= , CM000666.1:g.25158592T=	GRCh37
NC_000004.10:g.24767690T=	NCBI36
NG_028222.1:g.8613A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.274A= MANE Select	ENSP00000371535.2:p.Ile92=
ENST00000680581.1:c.274A=	ENSP00000506483.1:p.Ile92=
ENST00000680824.1:n.1490A=
ENST00000681071.1:n.566A=
ENST00000681166.1:n.1321A=
ENST00000681341.1:n.1415A=
ENST00000681640.1:n.368A=
ENST00000681948.1:c.529A=	ENSP00000505991.1:p.Ile177=
ENST00000358971.7:c.*72A=	ENSP00000351857.3:n.*72A=
ENST00000382103.6:c.274A=	ENSP00000371535.2:p.Ile92=
ENST00000514585.5:c.119A=	ENSP00000421880.1:p.His40=
NM_016955.3:c.274A=	NP_058651.3:p.Ile92=
XM_005248168.2:c.37A=	XP_005248225.1:p.Ile13=
XM_006713965.2:c.94A=	XP_006714028.1:p.Ile32=
XM_011513846.1:c.271A=	XP_011512148.1:p.Ile91=
XM_011513847.1:c.241A=	XP_011512149.1:p.Ile81=
XM_011513848.1:c.94A=	XP_011512150.1:p.Ile32=
XM_011513846.2:c.271A=	XP_011512148.1:p.Ile91=
XM_011513847.2:c.241A=	XP_011512149.1:p.Ile81=
XM_017008277.1:c.529A=	XP_016863766.1:p.Ile177=
XM_017008278.1:c.-150A=	XP_016863767.1:n.-150A=
NM_016955.4:c.274A= MANE Select	NP_058651.3:p.Ile92=