Canonical Allele Identifier: CA1445223220

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144778C= , CM000666.2:g.25144778C=	GRCh38
NC_000004.11:g.25146400C= , CM000666.1:g.25146400C=	GRCh37
NC_000004.10:g.24755498C=	NCBI36
NG_028222.1:g.20805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1022G= MANE Select	ENSP00000371535.2:p.Arg341=
ENST00000680581.1:c.1022G=	ENSP00000506483.1:p.Arg341=
ENST00000680824.1:n.2238G=
ENST00000681071.1:n.1314G=
ENST00000681341.1:n.2163G=
ENST00000681948.1:c.1277G=	ENSP00000505991.1:p.Arg426=
ENST00000358971.7:c.*820G=	ENSP00000351857.3:n.*820G=
ENST00000382103.6:c.1022G=	ENSP00000371535.2:p.Arg341=
ENST00000503150.1:c.304G=
ENST00000505513.1:n.322G=
ENST00000514585.5:c.*723G=	ENSP00000421880.1:n.*723G=
NM_016955.3:c.1022G=	NP_058651.3:p.Arg341=
XM_005248168.2:c.785G=	XP_005248225.1:p.Arg262=
XM_006713965.2:c.842G=	XP_006714028.1:p.Arg281=
XM_011513846.1:c.1019G=	XP_011512148.1:p.Arg340=
XM_011513847.1:c.989G=	XP_011512149.1:p.Arg330=
XM_011513848.1:c.842G=	XP_011512150.1:p.Arg281=
XM_011513846.2:c.1019G=	XP_011512148.1:p.Arg340=
XM_011513847.2:c.989G=	XP_011512149.1:p.Arg330=
XM_017008277.1:c.1277G=	XP_016863766.1:p.Arg426=
XM_017008278.1:c.599G=	XP_016863767.1:p.Arg200=
NM_016955.4:c.1022G= MANE Select	NP_058651.3:p.Arg341=