Canonical Allele Identifier: CA1666700172

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137868805C= , CM000668.2:g.137868805C=	GRCh38
NC_000006.11:g.138189942C= , CM000668.1:g.138189942C=	GRCh37
NC_000006.10:g.138231635C=	NCBI36
NG_032761.1:g.6362C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001270508.2:c.-16+1263C= MANE Select	NP_001257437.1:n.-16+1263C=
ENST00000612899.5:c.-16+1263C= MANE Select	ENSP00000481570.1:n.-16+1263C=
NM_001270507.1:c.-16+1287C=	NP_001257436.1:n.-16+1287C=
NM_001270507.2:c.-16+1287C=	NP_001257436.1:n.-16+1287C=
NM_001270508.1:c.-16+1263C=	NP_001257437.1:n.-16+1263C=
NM_006290.3:c.-16+1311C=	NP_006281.1:n.-16+1311C=
NM_006290.4:c.-16+1311C=	NP_006281.1:n.-16+1311C=
ENST00000237289.8:c.-16+1311C=	ENSP00000237289.4:n.-16+1311C=
ENST00000420009.5:c.-16+1287C=	ENSP00000401562.1:n.-16+1287C=
ENST00000420009.6:c.-16+1287C=	ENSP00000401562.2:n.-16+1287C=
ENST00000421450.1:c.-16+1263C=	ENSP00000393577.1:n.-16+1263C=
ENST00000421450.2:c.-16+1263C=	ENSP00000393577.2:n.-16+1263C=
ENST00000433680.1:c.-16+1069C=	ENSP00000409845.1:n.-16+1069C=
ENST00000433680.2:c.-16+1069C=	ENSP00000409845.2:n.-16+1069C=
ENST00000612899.4:c.-16+1263C=	ENSP00000481570.1:n.-16+1263C=
ENST00000698329.1:n.174+1311C=
ENST00000711061.1:c.-16+1263C=	ENSP00000518561.1:n.-16+1263C=
XM_011536095.1:c.-16+1833C=	XP_011534397.1:n.-16+1833C=
XM_011536096.1:c.-16+1263C=	XP_011534398.1:n.-16+1263C=
XM_011536096.2:c.-16+1263C=	XP_011534398.1:n.-16+1263C=
XM_024446532.1:c.-2123C=	XP_024302300.1:n.-2123C=
XM_024446533.1:c.-16+564C=	XP_024302301.1:n.-16+564C=