Canonical Allele Identifier: CA1666705464

Gene: TNFAIP3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137881704C= , CM000668.2:g.137881704C=	GRCh38
NC_000006.11:g.138202841C= , CM000668.1:g.138202841C=	GRCh37
NC_000006.10:g.138244534C=	NCBI36
NG_032761.1:g.19261C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001270508.2:c.*385C= MANE Select	NP_001257437.1:n.*385C=
ENST00000612899.5:c.*385C= MANE Select	ENSP00000481570.1:n.*385C=
NM_001270507.1:c.*385C=	NP_001257436.1:n.*385C=
NM_001270507.2:c.*385C=	NP_001257436.1:n.*385C=
NM_001270508.1:c.*385C=	NP_001257437.1:n.*385C=
NM_006290.3:c.*385C=	NP_006281.1:n.*385C=
NM_006290.4:c.*385C=	NP_006281.1:n.*385C=
ENST00000237289.8:c.*385C=	ENSP00000237289.4:n.*385C=
ENST00000420009.6:c.*385C=	ENSP00000401562.2:n.*385C=
ENST00000421450.2:c.*385C=	ENSP00000393577.2:n.*385C=
ENST00000433680.2:c.*385C=	ENSP00000409845.2:n.*385C=
ENST00000485192.2:n.3379C=
ENST00000612899.4:c.*385C=	ENSP00000481570.1:n.*385C=
ENST00000615468.4:c.*2112C=	ENSP00000479556.1:n.*2112C=
ENST00000620204.3:c.*746C=	ENSP00000481454.1:n.*746C=
ENST00000698329.1:n.3826C=
ENST00000711061.1:c.*2481C=	ENSP00000518561.1:n.*2481C=
XM_005267119.1:c.*385C=	XP_005267176.1:n.*385C=
XM_006715555.1:c.*385C=	XP_006715618.1:n.*385C=
XM_011536095.1:c.*385C=	XP_011534397.1:n.*385C=
XM_011536096.1:c.*506C=	XP_011534398.1:n.*506C=
XM_011536096.2:c.*506C=	XP_011534398.1:n.*506C=
XM_024446532.1:c.*385C=	XP_024302300.1:n.*385C=
XM_024446533.1:c.*385C=	XP_024302301.1:n.*385C=