Canonical Allele Identifier: CA4019837

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137881228G>A , CM000668.2:g.137881228G>A	GRCh38
NC_000006.11:g.138202365G>A , CM000668.1:g.138202365G>A	GRCh37
NC_000006.10:g.138244058G>A	NCBI36
NG_032761.1:g.18785G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001270508.2:c.2282G>A MANE Select	NP_001257437.1:p.Arg761His
ENST00000612899.5:c.2282G>A MANE Select	ENSP00000481570.1:p.Arg761His
NM_001270507.1:c.2282G>A	NP_001257436.1:p.Arg761His
NM_001270507.2:c.2282G>A	NP_001257436.1:p.Arg761His
NM_001270508.1:c.2282G>A	NP_001257437.1:p.Arg761His
NM_006290.3:c.2282G>A	NP_006281.1:p.Arg761His
NM_006290.4:c.2282G>A	NP_006281.1:p.Arg761His
ENST00000237289.8:c.2282G>A	ENSP00000237289.4:p.Arg761His
ENST00000420009.6:c.2282G>A	ENSP00000401562.2:p.Arg761His
ENST00000421450.2:c.2282G>A	ENSP00000393577.2:p.Arg761His
ENST00000433680.2:c.2282G>A	ENSP00000409845.2:p.Arg761His
ENST00000485192.2:n.2903G>A
ENST00000612899.4:c.2282G>A	ENSP00000481570.1:p.Arg761His
ENST00000615468.4:c.*1636G>A	ENSP00000479556.1:n.*1636G>A
ENST00000620204.3:c.*270G>A	ENSP00000481454.1:n.*270G>A
ENST00000698329.1:n.3350G>A
ENST00000711061.1:c.*2005G>A	ENSP00000518561.1:n.*2005G>A
XM_005267119.1:c.2282G>A	XP_005267176.1:p.Arg761His
XM_006715555.1:c.1643G>A	XP_006715618.1:p.Arg548His
XM_011536095.1:c.2282G>A	XP_011534397.1:p.Arg761His
XM_011536096.1:c.*30G>A	XP_011534398.1:n.*30G>A
XM_011536096.2:c.*30G>A	XP_011534398.1:n.*30G>A
XM_024446532.1:c.2282G>A	XP_024302300.1:p.Arg761His
XM_024446533.1:c.2282G>A	XP_024302301.1:p.Arg761His