Canonical Allele Identifier: CA1445223236

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144799T= , CM000666.2:g.25144799T=	GRCh38
NC_000004.11:g.25146421T= , CM000666.1:g.25146421T=	GRCh37
NC_000004.10:g.24755519T=	NCBI36
NG_028222.1:g.20784A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1001A= MANE Select	ENSP00000371535.2:p.Tyr334=
ENST00000680581.1:c.1001A=	ENSP00000506483.1:p.Tyr334=
ENST00000680824.1:n.2217A=
ENST00000681071.1:n.1293A=
ENST00000681341.1:n.2142A=
ENST00000681948.1:c.1256A=	ENSP00000505991.1:p.Tyr419=
ENST00000358971.7:c.*799A=	ENSP00000351857.3:n.*799A=
ENST00000382103.6:c.1001A=	ENSP00000371535.2:p.Tyr334=
ENST00000503150.1:c.283A=
ENST00000505513.1:n.301A=
ENST00000514585.5:c.*702A=	ENSP00000421880.1:n.*702A=
NM_016955.3:c.1001A=	NP_058651.3:p.Tyr334=
XM_005248168.2:c.764A=	XP_005248225.1:p.Tyr255=
XM_006713965.2:c.821A=	XP_006714028.1:p.Tyr274=
XM_011513846.1:c.998A=	XP_011512148.1:p.Tyr333=
XM_011513847.1:c.968A=	XP_011512149.1:p.Tyr323=
XM_011513848.1:c.821A=	XP_011512150.1:p.Tyr274=
XM_011513846.2:c.998A=	XP_011512148.1:p.Tyr333=
XM_011513847.2:c.968A=	XP_011512149.1:p.Tyr323=
XM_017008277.1:c.1256A=	XP_016863766.1:p.Tyr419=
XM_017008278.1:c.578A=	XP_016863767.1:p.Tyr193=
NM_016955.4:c.1001A= MANE Select	NP_058651.3:p.Tyr334=