Canonical Allele Identifier: CA2674974917

Gene: TNFAIP8

Linked Data

• gnomAD v4: 5-119393610-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119393610G>C , CM000667.2:g.119393610G>C	GRCh38
NC_000005.9:g.118729305G>C , CM000667.1:g.118729305G>C	GRCh37
NC_000005.8:g.118757204G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504771.3:c.*229G>C MANE Select	ENSP00000422245.1:n.*229G>C
ENST00000415806.2:c.*825G>C	ENSP00000408534.2:n.*825G>C
ENST00000503646.1:c.*229G>C	ENSP00000421848.1:n.*229G>C
ENST00000504771.2:c.*229G>C	ENSP00000422245.1:n.*229G>C
ENST00000513374.1:c.*229G>C	ENSP00000427424.1:n.*229G>C
NM_001077654.2:c.*229G>C	NP_001071122.1:n.*229G>C
NM_001286813.1:c.*229G>C	NP_001273742.1:n.*229G>C
NM_001286814.1:c.*229G>C	NP_001273743.1:n.*229G>C
NM_001286815.1:c.*229G>C	NP_001273744.1:n.*229G>C
NM_001286817.1:c.*229G>C	NP_001273746.1:n.*229G>C
NM_014350.3:c.*229G>C	NP_055165.2:n.*229G>C
XM_017009327.1:c.*229G>C	XP_016864816.1:n.*229G>C
XM_017009328.1:c.*229G>C	XP_016864817.1:n.*229G>C
NM_014350.4:c.*229G>C MANE Select	NP_055165.2:n.*229G>C
NM_001077654.3:c.*229G>C	NP_001071122.1:n.*229G>C
NM_001286813.2:c.*229G>C	NP_001273742.1:n.*229G>C
NM_001286815.2:c.*229G>C	NP_001273744.1:n.*229G>C
NM_001286817.2:c.*229G>C	NP_001273746.1:n.*229G>C