Canonical Allele Identifier: CA2802899005

Gene: TNFAIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137128T>G , CM000676.2:g.103137128T>G	GRCh38
NC_000014.8:g.103603465T>G , CM000676.1:g.103603465T>G	GRCh37
NC_000014.7:g.102673218T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333007.8:c.*1768T>G	ENSP00000332326.1:n.*1768T>G
ENST00000560869.6:c.*1768T>G MANE Select	ENSP00000452634.2:n.*1768T>G
ENST00000333007.5:c.*1768T>G	ENSP00000332326.1:n.*1768T>G
ENST00000560869.5:c.*1768T>G	ENSP00000452634.1:n.*1768T>G
ENST00000561217.1:n.299T>G
NM_006291.2:c.*1768T>G	NP_006282.2:n.*1768T>G
XM_006720243.2:c.*1125T>G	XP_006720306.1:n.*1125T>G
XM_011537112.1:c.*1125T>G	XP_011535414.1:n.*1125T>G
XM_011537113.1:c.*1125T>G	XP_011535415.1:n.*1125T>G
XM_011537114.1:c.*1768T>G	XP_011535416.1:n.*1768T>G
XM_006720243.3:c.*1125T>G	XP_006720306.1:n.*1125T>G
XM_011537112.2:c.*1125T>G	XP_011535414.1:n.*1125T>G
XM_011537113.2:c.*1125T>G	XP_011535415.1:n.*1125T>G
XM_011537114.2:c.*1768T>G	XP_011535416.1:n.*1768T>G
XM_017021616.1:c.*1125T>G	XP_016877105.1:n.*1125T>G
NM_006291.3:c.*1768T>G	NP_006282.2:n.*1768T>G
NM_001371220.1:c.*1125T>G	NP_001358149.1:n.*1125T>G
NM_001371221.1:c.*1125T>G	NP_001358150.1:n.*1125T>G
NM_006291.4:c.*1768T>G MANE Select	NP_006282.2:n.*1768T>G