Canonical Allele Identifier: CA148261518

Gene: TNFAIP3

Linked Data

• dbSNP Id: rs374509361
• gnomAD v2: 6-138198013-TTA-T
• gnomAD v3: 6-137876876-TTA-T
• gnomAD v4: 6-137876876-TTA-T
• MyVariant Identifiers: chr6:g.138198014_138198015del (hg19) ; chr6:g.137876877_137876878del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137876878_137876879del , CM000668.2:g.137876878_137876879del	GRCh38
NC_000006.11:g.138198015_138198016del , CM000668.1:g.138198015_138198016del	GRCh37
NC_000006.10:g.138239708_138239709del	NCBI36
NG_032761.1:g.14435_14436del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420009.6:c.806-198_806-197del	ENSP00000401562.2:n.806-198_806-197del
ENST00000711061.1:c.*529-198_*529-197del	ENSP00000518561.1:n.*529-198_*529-197del
ENST00000421450.2:c.806-198_806-197del	ENSP00000393577.2:n.806-198_806-197del
ENST00000433680.2:c.806-198_806-197del	ENSP00000409845.2:n.806-198_806-197del
ENST00000485192.2:n.1427-198_1427-197del
ENST00000698329.1:n.1155-198_1155-197del
ENST00000698330.1:n.296-1554_296-1553del
ENST00000612899.5:c.806-198_806-197del MANE Select	ENSP00000481570.1:n.806-198_806-197del
ENST00000237289.8:c.806-198_806-197del	ENSP00000237289.4:n.806-198_806-197del
ENST00000485192.1:n.330-198_330-197del
ENST00000612899.4:c.806-198_806-197del	ENSP00000481570.1:n.806-198_806-197del
ENST00000614035.4:c.806-198_806-197del	ENSP00000481122.2:n.806-198_806-197del
ENST00000615468.4:c.*160-198_*160-197del	ENSP00000479556.1:n.*160-198_*160-197del
ENST00000619035.4:c.806-198_806-197del	ENSP00000478438.1:n.806-198_806-197del
ENST00000620204.3:c.806-198_806-197del	ENSP00000481454.1:n.806-198_806-197del
ENST00000621150.3:c.806-198_806-197del	ENSP00000484332.2:n.806-198_806-197del
NM_001270507.1:c.806-198_806-197del	NP_001257436.1:n.806-198_806-197del
NM_001270508.1:c.806-198_806-197del	NP_001257437.1:n.806-198_806-197del
NM_006290.3:c.806-198_806-197del	NP_006281.1:n.806-198_806-197del
XM_005267119.1:c.806-198_806-197del	XP_005267176.1:n.806-198_806-197del
XM_006715555.1:c.167-198_167-197del	XP_006715618.1:n.167-198_167-197del
XM_011536095.1:c.806-198_806-197del	XP_011534397.1:n.806-198_806-197del
XM_011536096.1:c.806-198_806-197del	XP_011534398.1:n.806-198_806-197del
XM_011536096.2:c.806-198_806-197del	XP_011534398.1:n.806-198_806-197del
XM_024446532.1:c.806-198_806-197del	XP_024302300.1:n.806-198_806-197del
XM_024446533.1:c.806-198_806-197del	XP_024302301.1:n.806-198_806-197del
NM_001270508.2:c.806-198_806-197del MANE Select	NP_001257437.1:n.806-198_806-197del
NM_001270507.2:c.806-198_806-197del	NP_001257436.1:n.806-198_806-197del
NM_006290.4:c.806-198_806-197del	NP_006281.1:n.806-198_806-197del