Canonical Allele Identifier: CA1445223249

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144806T= , CM000666.2:g.25144806T=	GRCh38
NC_000004.11:g.25146428T= , CM000666.1:g.25146428T=	GRCh37
NC_000004.10:g.24755526T=	NCBI36
NG_028222.1:g.20777A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.994A= MANE Select	ENSP00000371535.2:p.Asn332=
ENST00000680581.1:c.994A=	ENSP00000506483.1:p.Asn332=
ENST00000680824.1:n.2210A=
ENST00000681071.1:n.1286A=
ENST00000681341.1:n.2135A=
ENST00000681948.1:c.1249A=	ENSP00000505991.1:p.Asn417=
ENST00000358971.7:c.*792A=	ENSP00000351857.3:n.*792A=
ENST00000382103.6:c.994A=	ENSP00000371535.2:p.Asn332=
ENST00000503150.1:c.276A=
ENST00000505513.1:n.294A=
ENST00000514585.5:c.*695A=	ENSP00000421880.1:n.*695A=
NM_016955.3:c.994A=	NP_058651.3:p.Asn332=
XM_005248168.2:c.757A=	XP_005248225.1:p.Asn253=
XM_006713965.2:c.814A=	XP_006714028.1:p.Asn272=
XM_011513846.1:c.991A=	XP_011512148.1:p.Asn331=
XM_011513847.1:c.961A=	XP_011512149.1:p.Asn321=
XM_011513848.1:c.814A=	XP_011512150.1:p.Asn272=
XM_011513846.2:c.991A=	XP_011512148.1:p.Asn331=
XM_011513847.2:c.961A=	XP_011512149.1:p.Asn321=
XM_017008277.1:c.1249A=	XP_016863766.1:p.Asn417=
XM_017008278.1:c.571A=	XP_016863767.1:p.Asn191=
NM_016955.4:c.994A= MANE Select	NP_058651.3:p.Asn332=