Canonical Allele Identifier: CA1445223214

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144775T= , CM000666.2:g.25144775T=	GRCh38
NC_000004.11:g.25146397T= , CM000666.1:g.25146397T=	GRCh37
NC_000004.10:g.24755495T=	NCBI36
NG_028222.1:g.20808A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1025A= MANE Select	ENSP00000371535.2:p.Lys342=
ENST00000680581.1:c.1025A=	ENSP00000506483.1:p.Lys342=
ENST00000680824.1:n.2241A=
ENST00000681071.1:n.1317A=
ENST00000681341.1:n.2166A=
ENST00000681948.1:c.1280A=	ENSP00000505991.1:p.Lys427=
ENST00000358971.7:c.*823A=	ENSP00000351857.3:n.*823A=
ENST00000382103.6:c.1025A=	ENSP00000371535.2:p.Lys342=
ENST00000503150.1:c.307A=
ENST00000505513.1:n.325A=
ENST00000514585.5:c.*726A=	ENSP00000421880.1:n.*726A=
NM_016955.3:c.1025A=	NP_058651.3:p.Lys342=
XM_005248168.2:c.788A=	XP_005248225.1:p.Lys263=
XM_006713965.2:c.845A=	XP_006714028.1:p.Lys282=
XM_011513846.1:c.1022A=	XP_011512148.1:p.Lys341=
XM_011513847.1:c.992A=	XP_011512149.1:p.Lys331=
XM_011513848.1:c.845A=	XP_011512150.1:p.Lys282=
XM_011513846.2:c.1022A=	XP_011512148.1:p.Lys341=
XM_011513847.2:c.992A=	XP_011512149.1:p.Lys331=
XM_017008277.1:c.1280A=	XP_016863766.1:p.Lys427=
XM_017008278.1:c.602A=	XP_016863767.1:p.Lys201=
NM_016955.4:c.1025A= MANE Select	NP_058651.3:p.Lys342=