Canonical Allele Identifier: CA1445223225

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144786T= , CM000666.2:g.25144786T=	GRCh38
NC_000004.11:g.25146408T= , CM000666.1:g.25146408T=	GRCh37
NC_000004.10:g.24755506T=	NCBI36
NG_028222.1:g.20797A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1014A= MANE Select	ENSP00000371535.2:p.Leu338=
ENST00000680581.1:c.1014A=	ENSP00000506483.1:p.Leu338=
ENST00000680824.1:n.2230A=
ENST00000681071.1:n.1306A=
ENST00000681341.1:n.2155A=
ENST00000681948.1:c.1269A=	ENSP00000505991.1:p.Leu423=
ENST00000358971.7:c.*812A=	ENSP00000351857.3:n.*812A=
ENST00000382103.6:c.1014A=	ENSP00000371535.2:p.Leu338=
ENST00000503150.1:c.296A=
ENST00000505513.1:n.314A=
ENST00000514585.5:c.*715A=	ENSP00000421880.1:n.*715A=
NM_016955.3:c.1014A=	NP_058651.3:p.Leu338=
XM_005248168.2:c.777A=	XP_005248225.1:p.Leu259=
XM_006713965.2:c.834A=	XP_006714028.1:p.Leu278=
XM_011513846.1:c.1011A=	XP_011512148.1:p.Leu337=
XM_011513847.1:c.981A=	XP_011512149.1:p.Leu327=
XM_011513848.1:c.834A=	XP_011512150.1:p.Leu278=
XM_011513846.2:c.1011A=	XP_011512148.1:p.Leu337=
XM_011513847.2:c.981A=	XP_011512149.1:p.Leu327=
XM_017008277.1:c.1269A=	XP_016863766.1:p.Leu423=
XM_017008278.1:c.591A=	XP_016863767.1:p.Leu197=
NM_016955.4:c.1014A= MANE Select	NP_058651.3:p.Leu338=