Canonical Allele Identifier: CA2160158399

Gene: TNFAIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103135941A= , CM000676.2:g.103135941A=	GRCh38
NC_000014.8:g.103602278A= , CM000676.1:g.103602278A=	GRCh37
NC_000014.7:g.102672031A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333007.8:c.*581A=	ENSP00000332326.1:n.*581A=
ENST00000560869.6:c.*581A= MANE Select	ENSP00000452634.2:n.*581A=
ENST00000333007.5:c.*581A=	ENSP00000332326.1:n.*581A=
ENST00000559255.1:c.669A=
ENST00000560869.5:c.*581A=	ENSP00000452634.1:n.*581A=
NM_006291.2:c.*581A=	NP_006282.2:n.*581A=
XM_006720243.2:c.2089A=	XP_006720306.1:p.Ile697=
XM_011537112.1:c.2089A=	XP_011535414.1:p.Ile697=
XM_011537113.1:c.2089A=	XP_011535415.1:p.Ile697=
XM_011537114.1:c.*581A=	XP_011535416.1:n.*581A=
XM_006720243.3:c.2089A=	XP_006720306.1:p.Ile697=
XM_011537112.2:c.2089A=	XP_011535414.1:p.Ile697=
XM_011537113.2:c.2089A=	XP_011535415.1:p.Ile697=
XM_011537114.2:c.*581A=	XP_011535416.1:n.*581A=
XM_017021616.1:c.2089A=	XP_016877105.1:p.Ile697=
NM_006291.3:c.*581A=	NP_006282.2:n.*581A=
NM_001371220.1:c.2089A=	NP_001358149.1:p.Ile697=
NM_001371221.1:c.2089A=	NP_001358150.1:p.Ile697=
NM_006291.4:c.*581A= MANE Select	NP_006282.2:n.*581A=