Canonical Allele Identifier: CA1445223340

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144938T= , CM000666.2:g.25144938T=	GRCh38
NC_000004.11:g.25146560T= , CM000666.1:g.25146560T=	GRCh37
NC_000004.10:g.24755658T=	NCBI36
NG_028222.1:g.20645A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.934+66A= MANE Select	ENSP00000371535.2:n.934+66A=
ENST00000680581.1:c.934+66A=	ENSP00000506483.1:n.934+66A=
ENST00000680824.1:n.2150+66A=
ENST00000681071.1:n.1226+66A=
ENST00000681341.1:n.2075+66A=
ENST00000681948.1:c.1189+66A=	ENSP00000505991.1:n.1189+66A=
ENST00000358971.7:c.*732+66A=	ENSP00000351857.3:n.*732+66A=
ENST00000382103.6:c.934+66A=	ENSP00000371535.2:n.934+66A=
ENST00000503150.1:c.217-73A=
ENST00000505513.1:n.235-73A=
ENST00000514585.5:c.*635+66A=	ENSP00000421880.1:n.*635+66A=
NM_016955.3:c.934+66A=	NP_058651.3:n.934+66A=
XM_005248168.2:c.697+66A=	XP_005248225.1:n.697+66A=
XM_006713965.2:c.754+66A=	XP_006714028.1:n.754+66A=
XM_011513846.1:c.931+66A=	XP_011512148.1:n.931+66A=
XM_011513847.1:c.901+66A=	XP_011512149.1:n.901+66A=
XM_011513848.1:c.754+66A=	XP_011512150.1:n.754+66A=
XM_011513846.2:c.931+66A=	XP_011512148.1:n.931+66A=
XM_011513847.2:c.901+66A=	XP_011512149.1:n.901+66A=
XM_017008277.1:c.1189+66A=	XP_016863766.1:n.1189+66A=
XM_017008278.1:c.511+66A=	XP_016863767.1:n.511+66A=
NM_016955.4:c.934+66A= MANE Select	NP_058651.3:n.934+66A=