Canonical Allele Identifier: CA1445223252

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144812C= , CM000666.2:g.25144812C=	GRCh38
NC_000004.11:g.25146434C= , CM000666.1:g.25146434C=	GRCh37
NC_000004.10:g.24755532C=	NCBI36
NG_028222.1:g.20771G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.988G= MANE Select	ENSP00000371535.2:p.Gly330=
ENST00000680581.1:c.988G=	ENSP00000506483.1:p.Gly330=
ENST00000680824.1:n.2204G=
ENST00000681071.1:n.1280G=
ENST00000681341.1:n.2129G=
ENST00000681948.1:c.1243G=	ENSP00000505991.1:p.Gly415=
ENST00000358971.7:c.*786G=	ENSP00000351857.3:n.*786G=
ENST00000382103.6:c.988G=	ENSP00000371535.2:p.Gly330=
ENST00000503150.1:c.270G=
ENST00000505513.1:n.288G=
ENST00000514585.5:c.*689G=	ENSP00000421880.1:n.*689G=
NM_016955.3:c.988G=	NP_058651.3:p.Gly330=
XM_005248168.2:c.751G=	XP_005248225.1:p.Gly251=
XM_006713965.2:c.808G=	XP_006714028.1:p.Gly270=
XM_011513846.1:c.985G=	XP_011512148.1:p.Gly329=
XM_011513847.1:c.955G=	XP_011512149.1:p.Gly319=
XM_011513848.1:c.808G=	XP_011512150.1:p.Gly270=
XM_011513846.2:c.985G=	XP_011512148.1:p.Gly329=
XM_011513847.2:c.955G=	XP_011512149.1:p.Gly319=
XM_017008277.1:c.1243G=	XP_016863766.1:p.Gly415=
XM_017008278.1:c.565G=	XP_016863767.1:p.Gly189=
NM_016955.4:c.988G= MANE Select	NP_058651.3:p.Gly330=