Canonical Allele Identifier: CA802717546

Gene: TNFAIP8

Linked Data

• dbSNP Id: rs1156656804
• gnomAD v3: 5-119393713-AT-A
• gnomAD v4: 5-119393713-AT-A
• MyVariant Identifiers: chr5:g.118729409del (hg19) ; chr5:g.119393714del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119393715del , CM000667.2:g.119393715del	GRCh38
NC_000005.9:g.118729410del , CM000667.1:g.118729410del	GRCh37
NC_000005.8:g.118757309del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504771.3:c.*334del MANE Select	ENSP00000422245.1:n.*334del
ENST00000415806.2:c.*930del	ENSP00000408534.2:n.*930del
ENST00000503646.1:c.*334del	ENSP00000421848.1:n.*334del
ENST00000504771.2:c.*334del	ENSP00000422245.1:n.*334del
ENST00000513374.1:c.*334del	ENSP00000427424.1:n.*334del
NM_001077654.2:c.*334del	NP_001071122.1:n.*334del
NM_001286813.1:c.*334del	NP_001273742.1:n.*334del
NM_001286814.1:c.*334del	NP_001273743.1:n.*334del
NM_001286815.1:c.*334del	NP_001273744.1:n.*334del
NM_001286817.1:c.*334del	NP_001273746.1:n.*334del
NM_014350.3:c.*334del	NP_055165.2:n.*334del
XM_017009327.1:c.*334del	XP_016864816.1:n.*334del
XM_017009328.1:c.*334del	XP_016864817.1:n.*334del
NM_014350.4:c.*334del MANE Select	NP_055165.2:n.*334del
NM_001077654.3:c.*334del	NP_001071122.1:n.*334del
NM_001286813.2:c.*334del	NP_001273742.1:n.*334del
NM_001286815.2:c.*334del	NP_001273744.1:n.*334del
NM_001286817.2:c.*334del	NP_001273746.1:n.*334del