Canonical Allele Identifier: CA365793699

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137879273G>A , CM000668.2:g.137879273G>A	GRCh38
NC_000006.11:g.138200410G>A , CM000668.1:g.138200410G>A	GRCh37
NC_000006.10:g.138242103G>A	NCBI36
NG_032761.1:g.16830G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.1828G>A	ENSP00000401562.2:p.Ala610Thr
ENST00000711061.1:c.*1551G>A	ENSP00000518561.1:n.*1551G>A
ENST00000421450.2:c.1828G>A	ENSP00000393577.2:p.Ala610Thr
ENST00000433680.2:c.1828G>A	ENSP00000409845.2:p.Ala610Thr
ENST00000485192.2:n.2449G>A
ENST00000698329.1:n.2177G>A
ENST00000612899.5:c.1828G>A MANE Select	ENSP00000481570.1:p.Ala610Thr
ENST00000237289.8:c.1828G>A	ENSP00000237289.4:p.Ala610Thr
ENST00000612899.4:c.1828G>A	ENSP00000481570.1:p.Ala610Thr
ENST00000615468.4:c.*1182G>A	ENSP00000479556.1:n.*1182G>A
ENST00000619035.4:c.1828G>A	ENSP00000478438.1:p.Ala610Thr
ENST00000620204.3:c.1828G>A	ENSP00000481454.1:p.Ala610Thr
NM_001270507.1:c.1828G>A	NP_001257436.1:p.Ala610Thr
NM_001270508.1:c.1828G>A	NP_001257437.1:p.Ala610Thr
NM_006290.3:c.1828G>A	NP_006281.1:p.Ala610Thr
XM_005267119.1:c.1828G>A	XP_005267176.1:p.Ala610Thr
XM_006715555.1:c.1189G>A	XP_006715618.1:p.Ala397Thr
XM_011536095.1:c.1828G>A	XP_011534397.1:p.Ala610Thr
XM_011536096.1:c.1828G>A	XP_011534398.1:p.Ala610Thr
XM_011536096.2:c.1828G>A	XP_011534398.1:p.Ala610Thr
XM_024446532.1:c.1828G>A	XP_024302300.1:p.Ala610Thr
XM_024446533.1:c.1828G>A	XP_024302301.1:p.Ala610Thr
NM_001270508.2:c.1828G>A MANE Select	NP_001257437.1:p.Ala610Thr
NM_001270507.2:c.1828G>A	NP_001257436.1:p.Ala610Thr
NM_006290.4:c.1828G>A	NP_006281.1:p.Ala610Thr