Canonical Allele Identifier: CA1666703235

Gene: TNFAIP3

Linked Data

• ClinVar Variation Id: 1003848
• ClinVar RCV Id: RCV001300457
• dbSNP Id: rs1776240203

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137876171G>A , CM000668.2:g.137876171G>A	GRCh38
NC_000006.11:g.138197308G>A , CM000668.1:g.138197308G>A	GRCh37
NC_000006.10:g.138239001G>A	NCBI36
NG_032761.1:g.13728G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.805+5G>A	ENSP00000401562.2:n.805+5G>A
ENST00000711061.1:c.*528+5G>A	ENSP00000518561.1:n.*528+5G>A
ENST00000421450.2:c.805+5G>A	ENSP00000393577.2:n.805+5G>A
ENST00000433680.2:c.805+5G>A	ENSP00000409845.2:n.805+5G>A
ENST00000485192.2:n.1426+5G>A
ENST00000698329.1:n.1154+5G>A
ENST00000698330.1:n.296-2261G>A
ENST00000612899.5:c.805+5G>A MANE Select	ENSP00000481570.1:n.805+5G>A
ENST00000237289.8:c.805+5G>A	ENSP00000237289.4:n.805+5G>A
ENST00000485192.1:n.329+5G>A
ENST00000612899.4:c.805+5G>A	ENSP00000481570.1:n.805+5G>A
ENST00000614035.4:c.805+5G>A	ENSP00000481122.2:n.805+5G>A
ENST00000615468.4:c.*159+5G>A	ENSP00000479556.1:n.*159+5G>A
ENST00000619035.4:c.805+5G>A	ENSP00000478438.1:n.805+5G>A
ENST00000620204.3:c.805+5G>A	ENSP00000481454.1:n.805+5G>A
ENST00000621150.3:c.805+5G>A	ENSP00000484332.2:n.805+5G>A
NM_001270507.1:c.805+5G>A	NP_001257436.1:n.805+5G>A
NM_001270508.1:c.805+5G>A	NP_001257437.1:n.805+5G>A
NM_006290.3:c.805+5G>A	NP_006281.1:n.805+5G>A
XM_005267119.1:c.805+5G>A	XP_005267176.1:n.805+5G>A
XM_006715555.1:c.166+5G>A	XP_006715618.1:n.166+5G>A
XM_011536095.1:c.805+5G>A	XP_011534397.1:n.805+5G>A
XM_011536096.1:c.805+5G>A	XP_011534398.1:n.805+5G>A
XM_011536096.2:c.805+5G>A	XP_011534398.1:n.805+5G>A
XM_024446532.1:c.805+5G>A	XP_024302300.1:n.805+5G>A
XM_024446533.1:c.805+5G>A	XP_024302301.1:n.805+5G>A
NM_001270508.2:c.805+5G>A MANE Select	NP_001257437.1:n.805+5G>A
NM_001270507.2:c.805+5G>A	NP_001257436.1:n.805+5G>A
NM_006290.4:c.805+5G>A	NP_006281.1:n.805+5G>A