Canonical Allele Identifier: CA1445207417

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156340T= , CM000666.2:g.25156340T=	GRCh38
NC_000004.11:g.25157962T= , CM000666.1:g.25157962T=	GRCh37
NC_000004.10:g.24767060T=	NCBI36
NG_028222.1:g.9243A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-145A= MANE Select	ENSP00000371535.2:n.389-145A=
ENST00000680581.1:c.389-145A=	ENSP00000506483.1:n.389-145A=
ENST00000680824.1:n.1605-145A=
ENST00000681071.1:n.681-145A=
ENST00000681166.1:n.1436-145A=
ENST00000681341.1:n.1530-145A=
ENST00000681640.1:n.483-145A=
ENST00000681948.1:c.644-145A=	ENSP00000505991.1:n.644-145A=
ENST00000358971.7:c.*187-145A=	ENSP00000351857.3:n.*187-145A=
ENST00000382103.6:c.389-145A=	ENSP00000371535.2:n.389-145A=
ENST00000514585.5:c.*90-145A=	ENSP00000421880.1:n.*90-145A=
NM_016955.3:c.389-145A=	NP_058651.3:n.389-145A=
XM_005248168.2:c.152-145A=	XP_005248225.1:n.152-145A=
XM_006713965.2:c.209-145A=	XP_006714028.1:n.209-145A=
XM_011513846.1:c.386-145A=	XP_011512148.1:n.386-145A=
XM_011513847.1:c.356-145A=	XP_011512149.1:n.356-145A=
XM_011513848.1:c.209-145A=	XP_011512150.1:n.209-145A=
XM_011513846.2:c.386-145A=	XP_011512148.1:n.386-145A=
XM_011513847.2:c.356-145A=	XP_011512149.1:n.356-145A=
XM_017008277.1:c.644-145A=	XP_016863766.1:n.644-145A=
XM_017008278.1:c.-35-145A=	XP_016863767.1:n.-35-145A=
NM_016955.4:c.389-145A= MANE Select	NP_058651.3:n.389-145A=