Canonical Allele Identifier: CA1445204429

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120862A= , CM000666.2:g.25120862A=	GRCh38
NC_000004.11:g.25122484A= , CM000666.1:g.25122484A=	GRCh37
NC_000004.10:g.24731582A=	NCBI36
NG_028222.1:g.44721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3069T= MANE Select	ENSP00000371535.2:n.*3069T=
ENST00000680581.1:c.*3449T=	ENSP00000506483.1:n.*3449T=
ENST00000680824.1:n.5791T=
ENST00000681071.1:n.4867T=
ENST00000681341.1:n.5622T=
ENST00000681374.1:n.3931T=
ENST00000681948.1:c.*3069T=	ENSP00000505991.1:n.*3069T=
ENST00000382103.6:c.*3069T=	ENSP00000371535.2:n.*3069T=
NM_016955.3:c.*3069T=	NP_058651.3:n.*3069T=
XM_005248168.2:c.*3069T=	XP_005248225.1:n.*3069T=
XM_006713965.2:c.*3069T=	XP_006714028.1:n.*3069T=
XM_011513846.1:c.*3069T=	XP_011512148.1:n.*3069T=
XM_011513847.1:c.*3069T=	XP_011512149.1:n.*3069T=
XM_011513848.1:c.*3069T=	XP_011512150.1:n.*3069T=
XM_011513846.2:c.*3069T=	XP_011512148.1:n.*3069T=
XM_011513847.2:c.*3069T=	XP_011512149.1:n.*3069T=
XM_017008277.1:c.*3069T=	XP_016863766.1:n.*3069T=
XM_017008278.1:c.*3069T=	XP_016863767.1:n.*3069T=
NM_016955.4:c.*3069T= MANE Select	NP_058651.3:n.*3069T=