Canonical Allele Identifier: CA1666703527

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137876910_137876911delinsAT , CM000668.2:g.137876910_137876911delinsAT	GRCh38
NC_000006.11:g.138198047_138198048delinsAT , CM000668.1:g.138198047_138198048delinsAT	GRCh37
NC_000006.10:g.138239740_138239741delinsAT	NCBI36
NG_032761.1:g.14467_14468delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.806-166_806-165delinsAT	ENSP00000401562.2:n.806-166_806-165delinsAT
ENST00000711061.1:c.*529-166_*529-165delinsAT	ENSP00000518561.1:n.*529-166_*529-165delinsAT
ENST00000421450.2:c.806-166_806-165delinsAT	ENSP00000393577.2:n.806-166_806-165delinsAT
ENST00000433680.2:c.806-166_806-165delinsAT	ENSP00000409845.2:n.806-166_806-165delinsAT
ENST00000485192.2:n.1427-166_1427-165delinsAT
ENST00000698329.1:n.1155-166_1155-165delinsAT
ENST00000698330.1:n.296-1522_296-1521delinsAT
ENST00000612899.5:c.806-166_806-165delinsAT MANE Select	ENSP00000481570.1:n.806-166_806-165delinsAT
ENST00000237289.8:c.806-166_806-165delinsAT	ENSP00000237289.4:n.806-166_806-165delinsAT
ENST00000485192.1:n.330-166_330-165delinsAT
ENST00000612899.4:c.806-166_806-165delinsAT	ENSP00000481570.1:n.806-166_806-165delinsAT
ENST00000614035.4:c.806-166_806-165delinsAT	ENSP00000481122.2:n.806-166_806-165delinsAT
ENST00000615468.4:c.*160-166_*160-165delinsAT	ENSP00000479556.1:n.*160-166_*160-165delinsAT
ENST00000619035.4:c.806-166_806-165delinsAT	ENSP00000478438.1:n.806-166_806-165delinsAT
ENST00000620204.3:c.806-166_806-165delinsAT	ENSP00000481454.1:n.806-166_806-165delinsAT
ENST00000621150.3:c.806-166_806-165delinsAT	ENSP00000484332.2:n.806-166_806-165delinsAT
NM_001270507.1:c.806-166_806-165delinsAT	NP_001257436.1:n.806-166_806-165delinsAT
NM_001270508.1:c.806-166_806-165delinsAT	NP_001257437.1:n.806-166_806-165delinsAT
NM_006290.3:c.806-166_806-165delinsAT	NP_006281.1:n.806-166_806-165delinsAT
XM_005267119.1:c.806-166_806-165delinsAT	XP_005267176.1:n.806-166_806-165delinsAT
XM_006715555.1:c.167-166_167-165delinsAT	XP_006715618.1:n.167-166_167-165delinsAT
XM_011536095.1:c.806-166_806-165delinsAT	XP_011534397.1:n.806-166_806-165delinsAT
XM_011536096.1:c.806-166_806-165delinsAT	XP_011534398.1:n.806-166_806-165delinsAT
XM_011536096.2:c.806-166_806-165delinsAT	XP_011534398.1:n.806-166_806-165delinsAT
XM_024446532.1:c.806-166_806-165delinsAT	XP_024302300.1:n.806-166_806-165delinsAT
XM_024446533.1:c.806-166_806-165delinsAT	XP_024302301.1:n.806-166_806-165delinsAT
NM_001270508.2:c.806-166_806-165delinsAT MANE Select	NP_001257437.1:n.806-166_806-165delinsAT
NM_001270507.2:c.806-166_806-165delinsAT	NP_001257436.1:n.806-166_806-165delinsAT
NM_006290.4:c.806-166_806-165delinsAT	NP_006281.1:n.806-166_806-165delinsAT