Canonical Allele Identifier: CA365784360
Community Standard Title: NM_001270508.2(TNFAIP3):c.738C>G (p.Tyr246Ter)
Gene: TNFAIP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137876099C>G , CM000668.2:g.137876099C>G GRCh38
NC_000006.11:g.138197236C>G , CM000668.1:g.138197236C>G GRCh37
NC_000006.10:g.138238929C>G NCBI36
NG_032761.1:g.13656C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001270508.2:c.738C>G MANE Select NP_001257437.1:p.Tyr246Ter
ENST00000612899.5:c.738C>G MANE Select ENSP00000481570.1:p.Tyr246Ter
NM_001270507.1:c.738C>G NP_001257436.1:p.Tyr246Ter
NM_001270507.2:c.738C>G NP_001257436.1:p.Tyr246Ter
NM_001270508.1:c.738C>G NP_001257437.1:p.Tyr246Ter
NM_006290.3:c.738C>G NP_006281.1:p.Tyr246Ter
NM_006290.4:c.738C>G NP_006281.1:p.Tyr246Ter
ENST00000237289.8:c.738C>G ENSP00000237289.4:p.Tyr246Ter
ENST00000420009.6:c.738C>G ENSP00000401562.2:p.Tyr246Ter
ENST00000421450.2:c.738C>G ENSP00000393577.2:p.Tyr246Ter
ENST00000433680.2:c.738C>G ENSP00000409845.2:p.Tyr246Ter
ENST00000485192.1:n.262C>G
ENST00000485192.2:n.1359C>G
ENST00000612899.4:c.738C>G ENSP00000481570.1:p.Tyr246Ter
ENST00000614035.4:c.738C>G ENSP00000481122.2:p.Tyr246Ter
ENST00000615468.4:c.*92C>G ENSP00000479556.1:n.*92C>G
ENST00000619035.4:c.738C>G ENSP00000478438.1:p.Tyr246Ter
ENST00000620204.3:c.738C>G ENSP00000481454.1:p.Tyr246Ter
ENST00000621150.3:c.738C>G ENSP00000484332.2:p.Tyr246Ter
ENST00000698329.1:n.1087C>G
ENST00000698330.1:n.296-2333C>G
ENST00000711061.1:c.*461C>G ENSP00000518561.1:n.*461C>G
XM_005267119.1:c.738C>G XP_005267176.1:p.Tyr246Ter
XM_006715555.1:c.99C>G XP_006715618.1:p.Tyr33Ter
XM_011536095.1:c.738C>G XP_011534397.1:p.Tyr246Ter
XM_011536096.1:c.738C>G XP_011534398.1:p.Tyr246Ter
XM_011536096.2:c.738C>G XP_011534398.1:p.Tyr246Ter
XM_024446532.1:c.738C>G XP_024302300.1:p.Tyr246Ter
XM_024446533.1:c.738C>G XP_024302301.1:p.Tyr246Ter