Canonical Allele Identifier: CA1666703505

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137876876_137876878delinsTTA , CM000668.2:g.137876876_137876878delinsTTA	GRCh38
NC_000006.11:g.138198013_138198015delinsTTA , CM000668.1:g.138198013_138198015delinsTTA	GRCh37
NC_000006.10:g.138239706_138239708delinsTTA	NCBI36
NG_032761.1:g.14433_14435delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.806-200_806-198delinsTTA	ENSP00000401562.2:n.806-200_806-198delinsTTA
ENST00000711061.1:c.*529-200_*529-198delinsTTA	ENSP00000518561.1:n.*529-200_*529-198delinsTTA
ENST00000421450.2:c.806-200_806-198delinsTTA	ENSP00000393577.2:n.806-200_806-198delinsTTA
ENST00000433680.2:c.806-200_806-198delinsTTA	ENSP00000409845.2:n.806-200_806-198delinsTTA
ENST00000485192.2:n.1427-200_1427-198delinsTTA
ENST00000698329.1:n.1155-200_1155-198delinsTTA
ENST00000698330.1:n.296-1556_296-1554delinsTTA
ENST00000612899.5:c.806-200_806-198delinsTTA MANE Select	ENSP00000481570.1:n.806-200_806-198delinsTTA
ENST00000237289.8:c.806-200_806-198delinsTTA	ENSP00000237289.4:n.806-200_806-198delinsTTA
ENST00000485192.1:n.330-200_330-198delinsTTA
ENST00000612899.4:c.806-200_806-198delinsTTA	ENSP00000481570.1:n.806-200_806-198delinsTTA
ENST00000614035.4:c.806-200_806-198delinsTTA	ENSP00000481122.2:n.806-200_806-198delinsTTA
ENST00000615468.4:c.*160-200_*160-198delinsTTA	ENSP00000479556.1:n.*160-200_*160-198delinsTTA
ENST00000619035.4:c.806-200_806-198delinsTTA	ENSP00000478438.1:n.806-200_806-198delinsTTA
ENST00000620204.3:c.806-200_806-198delinsTTA	ENSP00000481454.1:n.806-200_806-198delinsTTA
ENST00000621150.3:c.806-200_806-198delinsTTA	ENSP00000484332.2:n.806-200_806-198delinsTTA
NM_001270507.1:c.806-200_806-198delinsTTA	NP_001257436.1:n.806-200_806-198delinsTTA
NM_001270508.1:c.806-200_806-198delinsTTA	NP_001257437.1:n.806-200_806-198delinsTTA
NM_006290.3:c.806-200_806-198delinsTTA	NP_006281.1:n.806-200_806-198delinsTTA
XM_005267119.1:c.806-200_806-198delinsTTA	XP_005267176.1:n.806-200_806-198delinsTTA
XM_006715555.1:c.167-200_167-198delinsTTA	XP_006715618.1:n.167-200_167-198delinsTTA
XM_011536095.1:c.806-200_806-198delinsTTA	XP_011534397.1:n.806-200_806-198delinsTTA
XM_011536096.1:c.806-200_806-198delinsTTA	XP_011534398.1:n.806-200_806-198delinsTTA
XM_011536096.2:c.806-200_806-198delinsTTA	XP_011534398.1:n.806-200_806-198delinsTTA
XM_024446532.1:c.806-200_806-198delinsTTA	XP_024302300.1:n.806-200_806-198delinsTTA
XM_024446533.1:c.806-200_806-198delinsTTA	XP_024302301.1:n.806-200_806-198delinsTTA
NM_001270508.2:c.806-200_806-198delinsTTA MANE Select	NP_001257437.1:n.806-200_806-198delinsTTA
NM_001270507.2:c.806-200_806-198delinsTTA	NP_001257436.1:n.806-200_806-198delinsTTA
NM_006290.4:c.806-200_806-198delinsTTA	NP_006281.1:n.806-200_806-198delinsTTA