Canonical Allele Identifier: CA2839111592

Gene: TNFAIP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103137215_103137229del , CM000676.2:g.103137215_103137229del	GRCh38
NC_000014.8:g.103603552_103603566del , CM000676.1:g.103603552_103603566del	GRCh37
NC_000014.7:g.102673305_102673319del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333007.8:c.*1855_*1869del	ENSP00000332326.1:n.*1855_*1869del
ENST00000560869.6:c.*1855_*1869del MANE Select	ENSP00000452634.2:n.*1855_*1869del
ENST00000333007.5:c.*1855_*1869del	ENSP00000332326.1:n.*1855_*1869del
ENST00000560869.5:c.*1855_*1869del	ENSP00000452634.1:n.*1855_*1869del
ENST00000561217.1:n.386_400del
NM_006291.2:c.*1855_*1869del	NP_006282.2:n.*1855_*1869del
XM_006720243.2:c.*1212_*1226del	XP_006720306.1:n.*1212_*1226del
XM_011537112.1:c.*1212_*1226del	XP_011535414.1:n.*1212_*1226del
XM_011537113.1:c.*1212_*1226del	XP_011535415.1:n.*1212_*1226del
XM_011537114.1:c.*1855_*1869del	XP_011535416.1:n.*1855_*1869del
XM_006720243.3:c.*1212_*1226del	XP_006720306.1:n.*1212_*1226del
XM_011537112.2:c.*1212_*1226del	XP_011535414.1:n.*1212_*1226del
XM_011537113.2:c.*1212_*1226del	XP_011535415.1:n.*1212_*1226del
XM_011537114.2:c.*1855_*1869del	XP_011535416.1:n.*1855_*1869del
XM_017021616.1:c.*1212_*1226del	XP_016877105.1:n.*1212_*1226del
NM_006291.3:c.*1855_*1869del	NP_006282.2:n.*1855_*1869del
NM_001371220.1:c.*1212_*1226del	NP_001358149.1:n.*1212_*1226del
NM_001371221.1:c.*1212_*1226del	NP_001358150.1:n.*1212_*1226del
NM_006291.4:c.*1855_*1869del MANE Select	NP_006282.2:n.*1855_*1869del