Canonical Allele Identifier: CA2160158994

Gene: TNFAIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137121C= , CM000676.2:g.103137121C=	GRCh38
NC_000014.8:g.103603458C= , CM000676.1:g.103603458C=	GRCh37
NC_000014.7:g.102673211C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333007.8:c.*1761C=	ENSP00000332326.1:n.*1761C=
ENST00000560869.6:c.*1761C= MANE Select	ENSP00000452634.2:n.*1761C=
ENST00000333007.5:c.*1761C=	ENSP00000332326.1:n.*1761C=
ENST00000560869.5:c.*1761C=	ENSP00000452634.1:n.*1761C=
ENST00000561217.1:n.292C=
NM_006291.2:c.*1761C=	NP_006282.2:n.*1761C=
XM_006720243.2:c.*1118C=	XP_006720306.1:n.*1118C=
XM_011537112.1:c.*1118C=	XP_011535414.1:n.*1118C=
XM_011537113.1:c.*1118C=	XP_011535415.1:n.*1118C=
XM_011537114.1:c.*1761C=	XP_011535416.1:n.*1761C=
XM_006720243.3:c.*1118C=	XP_006720306.1:n.*1118C=
XM_011537112.2:c.*1118C=	XP_011535414.1:n.*1118C=
XM_011537113.2:c.*1118C=	XP_011535415.1:n.*1118C=
XM_011537114.2:c.*1761C=	XP_011535416.1:n.*1761C=
XM_017021616.1:c.*1118C=	XP_016877105.1:n.*1118C=
NM_006291.3:c.*1761C=	NP_006282.2:n.*1761C=
NM_001371220.1:c.*1118C=	NP_001358149.1:n.*1118C=
NM_001371221.1:c.*1118C=	NP_001358150.1:n.*1118C=
NM_006291.4:c.*1761C= MANE Select	NP_006282.2:n.*1761C=