Canonical Allele Identifier: CA1666703549

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137876964_137876965delinsAC , CM000668.2:g.137876964_137876965delinsAC	GRCh38
NC_000006.11:g.138198101_138198102delinsAC , CM000668.1:g.138198101_138198102delinsAC	GRCh37
NC_000006.10:g.138239794_138239795delinsAC	NCBI36
NG_032761.1:g.14521_14522delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.806-112_806-111delinsAC	ENSP00000401562.2:n.806-112_806-111delinsAC
ENST00000711061.1:c.*529-112_*529-111delinsAC	ENSP00000518561.1:n.*529-112_*529-111delinsAC
ENST00000421450.2:c.806-112_806-111delinsAC	ENSP00000393577.2:n.806-112_806-111delinsAC
ENST00000433680.2:c.806-112_806-111delinsAC	ENSP00000409845.2:n.806-112_806-111delinsAC
ENST00000485192.2:n.1427-112_1427-111delinsAC
ENST00000698329.1:n.1155-112_1155-111delinsAC
ENST00000698330.1:n.296-1468_296-1467delinsAC
ENST00000612899.5:c.806-112_806-111delinsAC MANE Select	ENSP00000481570.1:n.806-112_806-111delinsAC
ENST00000237289.8:c.806-112_806-111delinsAC	ENSP00000237289.4:n.806-112_806-111delinsAC
ENST00000485192.1:n.330-112_330-111delinsAC
ENST00000612899.4:c.806-112_806-111delinsAC	ENSP00000481570.1:n.806-112_806-111delinsAC
ENST00000614035.4:c.806-112_806-111delinsAC	ENSP00000481122.2:n.806-112_806-111delinsAC
ENST00000615468.4:c.*160-112_*160-111delinsAC	ENSP00000479556.1:n.*160-112_*160-111delinsAC
ENST00000619035.4:c.806-112_806-111delinsAC	ENSP00000478438.1:n.806-112_806-111delinsAC
ENST00000620204.3:c.806-112_806-111delinsAC	ENSP00000481454.1:n.806-112_806-111delinsAC
ENST00000621150.3:c.806-112_806-111delinsAC	ENSP00000484332.2:n.806-112_806-111delinsAC
NM_001270507.1:c.806-112_806-111delinsAC	NP_001257436.1:n.806-112_806-111delinsAC
NM_001270508.1:c.806-112_806-111delinsAC	NP_001257437.1:n.806-112_806-111delinsAC
NM_006290.3:c.806-112_806-111delinsAC	NP_006281.1:n.806-112_806-111delinsAC
XM_005267119.1:c.806-112_806-111delinsAC	XP_005267176.1:n.806-112_806-111delinsAC
XM_006715555.1:c.167-112_167-111delinsAC	XP_006715618.1:n.167-112_167-111delinsAC
XM_011536095.1:c.806-112_806-111delinsAC	XP_011534397.1:n.806-112_806-111delinsAC
XM_011536096.1:c.806-112_806-111delinsAC	XP_011534398.1:n.806-112_806-111delinsAC
XM_011536096.2:c.806-112_806-111delinsAC	XP_011534398.1:n.806-112_806-111delinsAC
XM_024446532.1:c.806-112_806-111delinsAC	XP_024302300.1:n.806-112_806-111delinsAC
XM_024446533.1:c.806-112_806-111delinsAC	XP_024302301.1:n.806-112_806-111delinsAC
NM_001270508.2:c.806-112_806-111delinsAC MANE Select	NP_001257437.1:n.806-112_806-111delinsAC
NM_001270507.2:c.806-112_806-111delinsAC	NP_001257436.1:n.806-112_806-111delinsAC
NM_006290.4:c.806-112_806-111delinsAC	NP_006281.1:n.806-112_806-111delinsAC