Canonical Allele Identifier: CA1445208868

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156966T= , CM000666.2:g.25156966T=	GRCh38
NC_000004.11:g.25158588T= , CM000666.1:g.25158588T=	GRCh37
NC_000004.10:g.24767686T=	NCBI36
NG_028222.1:g.8617A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.278A= MANE Select	ENSP00000371535.2:p.His93=
ENST00000680581.1:c.278A=	ENSP00000506483.1:p.His93=
ENST00000680824.1:n.1494A=
ENST00000681071.1:n.570A=
ENST00000681166.1:n.1325A=
ENST00000681341.1:n.1419A=
ENST00000681640.1:n.372A=
ENST00000681948.1:c.533A=	ENSP00000505991.1:p.His178=
ENST00000358971.7:c.*76A=	ENSP00000351857.3:n.*76A=
ENST00000382103.6:c.278A=	ENSP00000371535.2:p.His93=
ENST00000514585.5:c.123A=	ENSP00000421880.1:p.Ser41=
NM_016955.3:c.278A=	NP_058651.3:p.His93=
XM_005248168.2:c.41A=	XP_005248225.1:p.His14=
XM_006713965.2:c.98A=	XP_006714028.1:p.His33=
XM_011513846.1:c.275A=	XP_011512148.1:p.His92=
XM_011513847.1:c.245A=	XP_011512149.1:p.His82=
XM_011513848.1:c.98A=	XP_011512150.1:p.His33=
XM_011513846.2:c.275A=	XP_011512148.1:p.His92=
XM_011513847.2:c.245A=	XP_011512149.1:p.His82=
XM_017008277.1:c.533A=	XP_016863766.1:p.His178=
XM_017008278.1:c.-146A=	XP_016863767.1:n.-146A=
NM_016955.4:c.278A= MANE Select	NP_058651.3:p.His93=