Canonical Allele Identifier: CA452240453
Gene: TNFAIP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2851225
ClinVar RCV Id: RCV003691040
dbSNP Id: rs1272733096

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137871512G>A , CM000668.2:g.137871512G>A GRCh38
NC_000006.11:g.138192649G>A , CM000668.1:g.138192649G>A GRCh37
NC_000006.10:g.138234342G>A NCBI36
NG_032761.1:g.9069G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420009.6:c.285G>A ENSP00000401562.2:p.Leu95=
ENST00000711061.1:c.285G>A ENSP00000518561.1:p.Leu95=
ENST00000421450.2:c.285G>A ENSP00000393577.2:p.Leu95=
ENST00000433680.2:c.285G>A ENSP00000409845.2:p.Leu95=
ENST00000485192.2:n.94G>A
ENST00000698329.1:n.474G>A
ENST00000698330.1:n.285G>A
ENST00000612899.5:c.285G>A MANE Select ENSP00000481570.1:p.Leu95=
ENST00000237289.8:c.285G>A ENSP00000237289.4:p.Leu95=
ENST00000420009.5:c.285G>A ENSP00000401562.1:p.Leu95=
ENST00000433680.1:c.285G>A ENSP00000409845.1:p.Leu95=
ENST00000612899.4:c.285G>A ENSP00000481570.1:p.Leu95=
ENST00000614035.4:c.285G>A ENSP00000481122.2:p.Leu95=
ENST00000615468.4:c.285G>A ENSP00000479556.1:p.Leu95=
ENST00000619035.4:c.285G>A ENSP00000478438.1:p.Leu95=
ENST00000620204.3:c.285G>A ENSP00000481454.1:p.Leu95=
ENST00000621150.3:c.285G>A ENSP00000484332.2:p.Leu95=
NM_001270507.1:c.285G>A NP_001257436.1:p.Leu95=
NM_001270508.1:c.285G>A NP_001257437.1:p.Leu95=
NM_006290.3:c.285G>A NP_006281.1:p.Leu95=
XM_005267119.1:c.285G>A XP_005267176.1:p.Leu95=
XM_006715555.1:c.-367G>A XP_006715618.1:n.-367G>A
XM_011536095.1:c.285G>A XP_011534397.1:p.Leu95=
XM_011536096.1:c.285G>A XP_011534398.1:p.Leu95=
XM_011536096.2:c.285G>A XP_011534398.1:p.Leu95=
XM_024446532.1:c.285G>A XP_024302300.1:p.Leu95=
XM_024446533.1:c.285G>A XP_024302301.1:p.Leu95=
NM_001270508.2:c.285G>A MANE Select NP_001257437.1:p.Leu95=
NM_001270507.2:c.285G>A NP_001257436.1:p.Leu95=
NM_006290.4:c.285G>A NP_006281.1:p.Leu95=