Canonical Allele Identifier: CA2160159086

Gene: TNFAIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137292G= , CM000676.2:g.103137292G=	GRCh38
NC_000014.8:g.103603629G= , CM000676.1:g.103603629G=	GRCh37
NC_000014.7:g.102673382G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333007.8:c.*1932G=	ENSP00000332326.1:n.*1932G=
ENST00000560869.6:c.*1932G= MANE Select	ENSP00000452634.2:n.*1932G=
ENST00000333007.5:c.*1932G=	ENSP00000332326.1:n.*1932G=
ENST00000560869.5:c.*1932G=	ENSP00000452634.1:n.*1932G=
ENST00000561217.1:n.463G=
NM_006291.2:c.*1932G=	NP_006282.2:n.*1932G=
XM_006720243.2:c.*1289G=	XP_006720306.1:n.*1289G=
XM_011537112.1:c.*1289G=	XP_011535414.1:n.*1289G=
XM_011537113.1:c.*1289G=	XP_011535415.1:n.*1289G=
XM_011537114.1:c.*1932G=	XP_011535416.1:n.*1932G=
XM_006720243.3:c.*1289G=	XP_006720306.1:n.*1289G=
XM_011537112.2:c.*1289G=	XP_011535414.1:n.*1289G=
XM_011537113.2:c.*1289G=	XP_011535415.1:n.*1289G=
XM_011537114.2:c.*1932G=	XP_011535416.1:n.*1932G=
XM_017021616.1:c.*1289G=	XP_016877105.1:n.*1289G=
NM_006291.3:c.*1932G=	NP_006282.2:n.*1932G=
NM_001371220.1:c.*1289G=	NP_001358149.1:n.*1289G=
NM_001371221.1:c.*1289G=	NP_001358150.1:n.*1289G=
NM_006291.4:c.*1932G= MANE Select	NP_006282.2:n.*1932G=