Canonical Allele Identifier: CA2674974891

Gene: TNFAIP8

Linked Data

• gnomAD v4: 5-119393594-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119393594G>A , CM000667.2:g.119393594G>A	GRCh38
NC_000005.9:g.118729289G>A , CM000667.1:g.118729289G>A	GRCh37
NC_000005.8:g.118757188G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504771.3:c.*213G>A MANE Select	ENSP00000422245.1:n.*213G>A
ENST00000415806.2:c.*809G>A	ENSP00000408534.2:n.*809G>A
ENST00000503646.1:c.*213G>A	ENSP00000421848.1:n.*213G>A
ENST00000504771.2:c.*213G>A	ENSP00000422245.1:n.*213G>A
ENST00000513374.1:c.*213G>A	ENSP00000427424.1:n.*213G>A
NM_001077654.2:c.*213G>A	NP_001071122.1:n.*213G>A
NM_001286813.1:c.*213G>A	NP_001273742.1:n.*213G>A
NM_001286814.1:c.*213G>A	NP_001273743.1:n.*213G>A
NM_001286815.1:c.*213G>A	NP_001273744.1:n.*213G>A
NM_001286817.1:c.*213G>A	NP_001273746.1:n.*213G>A
NM_014350.3:c.*213G>A	NP_055165.2:n.*213G>A
XM_017009327.1:c.*213G>A	XP_016864816.1:n.*213G>A
XM_017009328.1:c.*213G>A	XP_016864817.1:n.*213G>A
NM_014350.4:c.*213G>A MANE Select	NP_055165.2:n.*213G>A
NM_001077654.3:c.*213G>A	NP_001071122.1:n.*213G>A
NM_001286813.2:c.*213G>A	NP_001273742.1:n.*213G>A
NM_001286815.2:c.*213G>A	NP_001273744.1:n.*213G>A
NM_001286817.2:c.*213G>A	NP_001273746.1:n.*213G>A