Canonical Allele Identifier: CA648711097

Gene: SEPSECS

Linked Data

• COSMIC: COSN20091025

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120826_25120827insT , CM000666.2:g.25120826_25120827insT	GRCh38
NC_000004.11:g.25122448_25122449insT , CM000666.1:g.25122448_25122449insT	GRCh37
NC_000004.10:g.24731546_24731547insT	NCBI36
NG_028222.1:g.44756_44757insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3104_*3105insA MANE Select	ENSP00000371535.2:n.*3104_*3105insA
ENST00000680581.1:c.*3484_*3485insA	ENSP00000506483.1:n.*3484_*3485insA
ENST00000680824.1:n.5826_5827insA
ENST00000681071.1:n.4902_4903insA
ENST00000681341.1:n.5657_5658insA
ENST00000681374.1:n.3966_3967insA
ENST00000681948.1:c.*3104_*3105insA	ENSP00000505991.1:n.*3104_*3105insA
ENST00000382103.6:c.*3104_*3105insA	ENSP00000371535.2:n.*3104_*3105insA
NM_016955.3:c.*3104_*3105insA	NP_058651.3:n.*3104_*3105insA
XM_005248168.2:c.*3104_*3105insA	XP_005248225.1:n.*3104_*3105insA
XM_006713965.2:c.*3104_*3105insA	XP_006714028.1:n.*3104_*3105insA
XM_011513846.1:c.*3104_*3105insA	XP_011512148.1:n.*3104_*3105insA
XM_011513847.1:c.*3104_*3105insA	XP_011512149.1:n.*3104_*3105insA
XM_011513848.1:c.*3104_*3105insA	XP_011512150.1:n.*3104_*3105insA
XM_011513846.2:c.*3104_*3105insA	XP_011512148.1:n.*3104_*3105insA
XM_011513847.2:c.*3104_*3105insA	XP_011512149.1:n.*3104_*3105insA
XM_017008277.1:c.*3104_*3105insA	XP_016863766.1:n.*3104_*3105insA
XM_017008278.1:c.*3104_*3105insA	XP_016863767.1:n.*3104_*3105insA
NM_016955.4:c.*3104_*3105insA MANE Select	NP_058651.3:n.*3104_*3105insA