Canonical Allele Identifier: CA819589831
Gene: TNFAIP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137868747C>A , CM000668.2:g.137868747C>A GRCh38
NC_000006.11:g.138189884C>A , CM000668.1:g.138189884C>A GRCh37
NC_000006.10:g.138231577C>A NCBI36
NG_032761.1:g.6304C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000420009.6:c.-16+1229C>A ENSP00000401562.2:n.-16+1229C>A
ENST00000711061.1:c.-16+1205C>A ENSP00000518561.1:n.-16+1205C>A
ENST00000421450.2:c.-16+1205C>A ENSP00000393577.2:n.-16+1205C>A
ENST00000433680.2:c.-16+1011C>A ENSP00000409845.2:n.-16+1011C>A
ENST00000698329.1:n.174+1253C>A
ENST00000612899.5:c.-16+1205C>A MANE Select ENSP00000481570.1:n.-16+1205C>A
ENST00000237289.8:c.-16+1253C>A ENSP00000237289.4:n.-16+1253C>A
ENST00000420009.5:c.-16+1229C>A ENSP00000401562.1:n.-16+1229C>A
ENST00000421450.1:c.-16+1205C>A ENSP00000393577.1:n.-16+1205C>A
ENST00000433680.1:c.-16+1011C>A ENSP00000409845.1:n.-16+1011C>A
ENST00000612899.4:c.-16+1205C>A ENSP00000481570.1:n.-16+1205C>A
NM_001270507.1:c.-16+1229C>A NP_001257436.1:n.-16+1229C>A
NM_001270508.1:c.-16+1205C>A NP_001257437.1:n.-16+1205C>A
NM_006290.3:c.-16+1253C>A NP_006281.1:n.-16+1253C>A
XM_011536095.1:c.-16+1775C>A XP_011534397.1:n.-16+1775C>A
XM_011536096.1:c.-16+1205C>A XP_011534398.1:n.-16+1205C>A
XM_011536096.2:c.-16+1205C>A XP_011534398.1:n.-16+1205C>A
XM_024446532.1:c.-2181C>A XP_024302300.1:n.-2181C>A
XM_024446533.1:c.-16+506C>A XP_024302301.1:n.-16+506C>A
NM_001270508.2:c.-16+1205C>A MANE Select NP_001257437.1:n.-16+1205C>A
NM_001270507.2:c.-16+1229C>A NP_001257436.1:n.-16+1229C>A
NM_006290.4:c.-16+1253C>A NP_006281.1:n.-16+1253C>A
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