Canonical Allele Identifier: CA1666703592

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137877081C= , CM000668.2:g.137877081C=	GRCh38
NC_000006.11:g.138198218C= , CM000668.1:g.138198218C=	GRCh37
NC_000006.10:g.138239911C=	NCBI36
NG_032761.1:g.14638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.811C=	ENSP00000401562.2:p.Arg271=
ENST00000711061.1:c.*534C=	ENSP00000518561.1:n.*534C=
ENST00000421450.2:c.811C=	ENSP00000393577.2:p.Arg271=
ENST00000433680.2:c.811C=	ENSP00000409845.2:p.Arg271=
ENST00000485192.2:n.1432C=
ENST00000698329.1:n.1160C=
ENST00000698330.1:n.296-1351C=
ENST00000612899.5:c.811C= MANE Select	ENSP00000481570.1:p.Arg271=
ENST00000237289.8:c.811C=	ENSP00000237289.4:p.Arg271=
ENST00000485192.1:n.335C=
ENST00000612899.4:c.811C=	ENSP00000481570.1:p.Arg271=
ENST00000614035.4:c.811C=	ENSP00000481122.2:p.Arg271=
ENST00000615468.4:c.*165C=	ENSP00000479556.1:n.*165C=
ENST00000619035.4:c.811C=	ENSP00000478438.1:p.Arg271=
ENST00000620204.3:c.811C=	ENSP00000481454.1:p.Arg271=
ENST00000621150.3:c.811C=	ENSP00000484332.2:p.Arg271=
NM_001270507.1:c.811C=	NP_001257436.1:p.Arg271=
NM_001270508.1:c.811C=	NP_001257437.1:p.Arg271=
NM_006290.3:c.811C=	NP_006281.1:p.Arg271=
XM_005267119.1:c.811C=	XP_005267176.1:p.Arg271=
XM_006715555.1:c.172C=	XP_006715618.1:p.Arg58=
XM_011536095.1:c.811C=	XP_011534397.1:p.Arg271=
XM_011536096.1:c.811C=	XP_011534398.1:p.Arg271=
XM_011536096.2:c.811C=	XP_011534398.1:p.Arg271=
XM_024446532.1:c.811C=	XP_024302300.1:p.Arg271=
XM_024446533.1:c.811C=	XP_024302301.1:p.Arg271=
NM_001270508.2:c.811C= MANE Select	NP_001257437.1:p.Arg271=
NM_001270507.2:c.811C=	NP_001257436.1:p.Arg271=
NM_006290.4:c.811C=	NP_006281.1:p.Arg271=