Canonical Allele Identifier: CA1445223258

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144829A= , CM000666.2:g.25144829A=	GRCh38
NC_000004.11:g.25146451A= , CM000666.1:g.25146451A=	GRCh37
NC_000004.10:g.24755549A=	NCBI36
NG_028222.1:g.20754T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.971T= MANE Select	ENSP00000371535.2:p.Ile324=
ENST00000680581.1:c.971T=	ENSP00000506483.1:p.Ile324=
ENST00000680824.1:n.2187T=
ENST00000681071.1:n.1263T=
ENST00000681341.1:n.2112T=
ENST00000681948.1:c.1226T=	ENSP00000505991.1:p.Ile409=
ENST00000358971.7:c.*769T=	ENSP00000351857.3:n.*769T=
ENST00000382103.6:c.971T=	ENSP00000371535.2:p.Ile324=
ENST00000503150.1:c.253T=
ENST00000505513.1:n.271T=
ENST00000514585.5:c.*672T=	ENSP00000421880.1:n.*672T=
NM_016955.3:c.971T=	NP_058651.3:p.Ile324=
XM_005248168.2:c.734T=	XP_005248225.1:p.Ile245=
XM_006713965.2:c.791T=	XP_006714028.1:p.Ile264=
XM_011513846.1:c.968T=	XP_011512148.1:p.Ile323=
XM_011513847.1:c.938T=	XP_011512149.1:p.Ile313=
XM_011513848.1:c.791T=	XP_011512150.1:p.Ile264=
XM_011513846.2:c.968T=	XP_011512148.1:p.Ile323=
XM_011513847.2:c.938T=	XP_011512149.1:p.Ile313=
XM_017008277.1:c.1226T=	XP_016863766.1:p.Ile409=
XM_017008278.1:c.548T=	XP_016863767.1:p.Ile183=
NM_016955.4:c.971T= MANE Select	NP_058651.3:p.Ile324=