Canonical Allele Identifier: CA2580075108

Gene: TNFAIP3

Linked Data

• ClinVar Variation Id: 2032945
• ClinVar RCV Id: RCV002881554

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137875800del , CM000668.2:g.137875800del	GRCh38
NC_000006.11:g.138196937del , CM000668.1:g.138196937del	GRCh37
NC_000006.10:g.138238630del	NCBI36
NG_032761.1:g.13357del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.599del	ENSP00000401562.2:p.Cys200SerfsTer16
ENST00000711061.1:c.*322del	ENSP00000518561.1:n.*322del
ENST00000421450.2:c.599del	ENSP00000393577.2:p.Cys200SerfsTer16
ENST00000433680.2:c.599del	ENSP00000409845.2:p.Cys200SerfsTer16
ENST00000485192.2:n.1060del
ENST00000698329.1:n.788del
ENST00000698330.1:n.296-2632del
ENST00000612899.5:c.599del MANE Select	ENSP00000481570.1:p.Cys200SerfsTer16
ENST00000237289.8:c.599del	ENSP00000237289.4:p.Cys200SerfsTer16
ENST00000612899.4:c.599del	ENSP00000481570.1:p.Cys200SerfsTer16
ENST00000614035.4:c.599del	ENSP00000481122.2:p.Cys200SerfsTer16
ENST00000615468.4:c.598del	ENSP00000479556.1:p.Ala200GlnfsTer?
ENST00000619035.4:c.599del	ENSP00000478438.1:p.Cys200SerfsTer16
ENST00000620204.3:c.599del	ENSP00000481454.1:p.Cys200SerfsTer16
ENST00000621150.3:c.599del	ENSP00000484332.2:p.Cys200SerfsTer16
NM_001270507.1:c.599del	NP_001257436.1:p.Cys200SerfsTer16
NM_001270508.1:c.599del	NP_001257437.1:p.Cys200SerfsTer16
NM_006290.3:c.599del	NP_006281.1:p.Cys200SerfsTer16
XM_005267119.1:c.599del	XP_005267176.1:p.Cys200SerfsTer16
XM_006715555.1:c.-165-36del	XP_006715618.1:n.-165-36del
XM_011536095.1:c.599del	XP_011534397.1:p.Cys200SerfsTer16
XM_011536096.1:c.599del	XP_011534398.1:p.Cys200SerfsTer16
XM_011536096.2:c.599del	XP_011534398.1:p.Cys200SerfsTer16
XM_024446532.1:c.599del	XP_024302300.1:p.Cys200SerfsTer16
XM_024446533.1:c.599del	XP_024302301.1:p.Cys200SerfsTer16
NM_001270508.2:c.599del MANE Select	NP_001257437.1:p.Cys200SerfsTer16
NM_001270507.2:c.599del	NP_001257436.1:p.Cys200SerfsTer16
NM_006290.4:c.599del	NP_006281.1:p.Cys200SerfsTer16