Canonical Allele Identifier: CA1666703541

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137876952_137876953delinsGT , CM000668.2:g.137876952_137876953delinsGT	GRCh38
NC_000006.11:g.138198089_138198090delinsGT , CM000668.1:g.138198089_138198090delinsGT	GRCh37
NC_000006.10:g.138239782_138239783delinsGT	NCBI36
NG_032761.1:g.14509_14510delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.806-124_806-123delinsGT	ENSP00000401562.2:n.806-124_806-123delinsGT
ENST00000711061.1:c.*529-124_*529-123delinsGT	ENSP00000518561.1:n.*529-124_*529-123delinsGT
ENST00000421450.2:c.806-124_806-123delinsGT	ENSP00000393577.2:n.806-124_806-123delinsGT
ENST00000433680.2:c.806-124_806-123delinsGT	ENSP00000409845.2:n.806-124_806-123delinsGT
ENST00000485192.2:n.1427-124_1427-123delinsGT
ENST00000698329.1:n.1155-124_1155-123delinsGT
ENST00000698330.1:n.296-1480_296-1479delinsGT
ENST00000612899.5:c.806-124_806-123delinsGT MANE Select	ENSP00000481570.1:n.806-124_806-123delinsGT
ENST00000237289.8:c.806-124_806-123delinsGT	ENSP00000237289.4:n.806-124_806-123delinsGT
ENST00000485192.1:n.330-124_330-123delinsGT
ENST00000612899.4:c.806-124_806-123delinsGT	ENSP00000481570.1:n.806-124_806-123delinsGT
ENST00000614035.4:c.806-124_806-123delinsGT	ENSP00000481122.2:n.806-124_806-123delinsGT
ENST00000615468.4:c.*160-124_*160-123delinsGT	ENSP00000479556.1:n.*160-124_*160-123delinsGT
ENST00000619035.4:c.806-124_806-123delinsGT	ENSP00000478438.1:n.806-124_806-123delinsGT
ENST00000620204.3:c.806-124_806-123delinsGT	ENSP00000481454.1:n.806-124_806-123delinsGT
ENST00000621150.3:c.806-124_806-123delinsGT	ENSP00000484332.2:n.806-124_806-123delinsGT
NM_001270507.1:c.806-124_806-123delinsGT	NP_001257436.1:n.806-124_806-123delinsGT
NM_001270508.1:c.806-124_806-123delinsGT	NP_001257437.1:n.806-124_806-123delinsGT
NM_006290.3:c.806-124_806-123delinsGT	NP_006281.1:n.806-124_806-123delinsGT
XM_005267119.1:c.806-124_806-123delinsGT	XP_005267176.1:n.806-124_806-123delinsGT
XM_006715555.1:c.167-124_167-123delinsGT	XP_006715618.1:n.167-124_167-123delinsGT
XM_011536095.1:c.806-124_806-123delinsGT	XP_011534397.1:n.806-124_806-123delinsGT
XM_011536096.1:c.806-124_806-123delinsGT	XP_011534398.1:n.806-124_806-123delinsGT
XM_011536096.2:c.806-124_806-123delinsGT	XP_011534398.1:n.806-124_806-123delinsGT
XM_024446532.1:c.806-124_806-123delinsGT	XP_024302300.1:n.806-124_806-123delinsGT
XM_024446533.1:c.806-124_806-123delinsGT	XP_024302301.1:n.806-124_806-123delinsGT
NM_001270508.2:c.806-124_806-123delinsGT MANE Select	NP_001257437.1:n.806-124_806-123delinsGT
NM_001270507.2:c.806-124_806-123delinsGT	NP_001257436.1:n.806-124_806-123delinsGT
NM_006290.4:c.806-124_806-123delinsGT	NP_006281.1:n.806-124_806-123delinsGT