Canonical Allele Identifier: CA2626702251

Gene: TNFAIP2

Linked Data

• gnomAD v4: 14-103137216-CCGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137218_103137220del , CM000676.2:g.103137218_103137220del	GRCh38
NC_000014.8:g.103603555_103603557del , CM000676.1:g.103603555_103603557del	GRCh37
NC_000014.7:g.102673308_102673310del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000333007.8:c.*1858_*1860del	ENSP00000332326.1:n.*1858_*1860del
ENST00000560869.6:c.*1858_*1860del MANE Select	ENSP00000452634.2:n.*1858_*1860del
ENST00000333007.5:c.*1858_*1860del	ENSP00000332326.1:n.*1858_*1860del
ENST00000560869.5:c.*1858_*1860del	ENSP00000452634.1:n.*1858_*1860del
ENST00000561217.1:n.389_391del
NM_006291.2:c.*1858_*1860del	NP_006282.2:n.*1858_*1860del
XM_006720243.2:c.*1215_*1217del	XP_006720306.1:n.*1215_*1217del
XM_011537112.1:c.*1215_*1217del	XP_011535414.1:n.*1215_*1217del
XM_011537113.1:c.*1215_*1217del	XP_011535415.1:n.*1215_*1217del
XM_011537114.1:c.*1858_*1860del	XP_011535416.1:n.*1858_*1860del
XM_006720243.3:c.*1215_*1217del	XP_006720306.1:n.*1215_*1217del
XM_011537112.2:c.*1215_*1217del	XP_011535414.1:n.*1215_*1217del
XM_011537113.2:c.*1215_*1217del	XP_011535415.1:n.*1215_*1217del
XM_011537114.2:c.*1858_*1860del	XP_011535416.1:n.*1858_*1860del
XM_017021616.1:c.*1215_*1217del	XP_016877105.1:n.*1215_*1217del
NM_006291.3:c.*1858_*1860del	NP_006282.2:n.*1858_*1860del
NM_001371220.1:c.*1215_*1217del	NP_001358149.1:n.*1215_*1217del
NM_001371221.1:c.*1215_*1217del	NP_001358150.1:n.*1215_*1217del
NM_006291.4:c.*1858_*1860del MANE Select	NP_006282.2:n.*1858_*1860del