Canonical Allele Identifier: CA1666703593

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137877082G= , CM000668.2:g.137877082G=	GRCh38
NC_000006.11:g.138198219G= , CM000668.1:g.138198219G=	GRCh37
NC_000006.10:g.138239912G=	NCBI36
NG_032761.1:g.14639G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.812G=	ENSP00000401562.2:p.Arg271=
ENST00000711061.1:c.*535G=	ENSP00000518561.1:n.*535G=
ENST00000421450.2:c.812G=	ENSP00000393577.2:p.Arg271=
ENST00000433680.2:c.812G=	ENSP00000409845.2:p.Arg271=
ENST00000485192.2:n.1433G=
ENST00000698329.1:n.1161G=
ENST00000698330.1:n.296-1350G=
ENST00000612899.5:c.812G= MANE Select	ENSP00000481570.1:p.Arg271=
ENST00000237289.8:c.812G=	ENSP00000237289.4:p.Arg271=
ENST00000485192.1:n.336G=
ENST00000612899.4:c.812G=	ENSP00000481570.1:p.Arg271=
ENST00000614035.4:c.812G=	ENSP00000481122.2:p.Arg271=
ENST00000615468.4:c.*166G=	ENSP00000479556.1:n.*166G=
ENST00000619035.4:c.812G=	ENSP00000478438.1:p.Arg271=
ENST00000620204.3:c.812G=	ENSP00000481454.1:p.Arg271=
ENST00000621150.3:c.812G=	ENSP00000484332.2:p.Arg271=
NM_001270507.1:c.812G=	NP_001257436.1:p.Arg271=
NM_001270508.1:c.812G=	NP_001257437.1:p.Arg271=
NM_006290.3:c.812G=	NP_006281.1:p.Arg271=
XM_005267119.1:c.812G=	XP_005267176.1:p.Arg271=
XM_006715555.1:c.173G=	XP_006715618.1:p.Arg58=
XM_011536095.1:c.812G=	XP_011534397.1:p.Arg271=
XM_011536096.1:c.812G=	XP_011534398.1:p.Arg271=
XM_011536096.2:c.812G=	XP_011534398.1:p.Arg271=
XM_024446532.1:c.812G=	XP_024302300.1:p.Arg271=
XM_024446533.1:c.812G=	XP_024302301.1:p.Arg271=
NM_001270508.2:c.812G= MANE Select	NP_001257437.1:p.Arg271=
NM_001270507.2:c.812G=	NP_001257436.1:p.Arg271=
NM_006290.4:c.812G=	NP_006281.1:p.Arg271=