Canonical Allele Identifier: CA251339
Gene: TJP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69221310_69221313del , CM000671.2:g.69221310_69221313del GRCh38
NC_000009.11:g.71836226_71836229del , CM000671.1:g.71836226_71836229del GRCh37
NC_000009.10:g.71026046_71026049del NCBI36
NG_016342.1:g.105003_105006del
NG_016342.2:g.125404_125407del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348208.9:c.766_769del ENSP00000345893.4:p.Ala256ThrfsTer?
ENST00000377245.9:c.766_769del MANE Select ENSP00000366453.4:p.Ala256ThrfsTer?
ENST00000535702.6:c.778_781del ENSP00000442090.1:p.Ala260ThrfsTer?
ENST00000539225.2:c.859_862del ENSP00000438262.1:p.Ala287ThrfsTer?
ENST00000636247.1:n.845_848del
ENST00000636438.1:c.943_946del ENSP00000489860.1:p.Ala315ThrfsTer?
ENST00000642889.1:c.1153_1156del ENSP00000493780.1:p.Ala385ThrfsTer?
ENST00000643352.1:c.*954_*957del ENSP00000496488.1:n.*954_*957del
ENST00000645088.1:c.*1073_*1076del ENSP00000495447.1:n.*1073_*1076del
ENST00000647986.1:c.697_700del ENSP00000496877.1:p.Ala233ThrfsTer?
ENST00000648087.1:n.1083_1086del
ENST00000649114.1:c.766_769del ENSP00000497328.1:p.Ala256ThrfsTer?
ENST00000649134.1:c.778_781del ENSP00000498068.1:p.Ala260ThrfsTer?
ENST00000649783.1:n.790_793del
ENST00000649943.1:c.766_769del ENSP00000497539.1:p.Ala256ThrfsTer?
ENST00000650084.1:c.769_772del ENSP00000497861.1:p.Ala257ThrfsTer?
ENST00000650333.1:c.697_700del ENSP00000496791.1:p.Ala233ThrfsTer?
ENST00000650460.1:c.39_42del
ENST00000650522.1:n.790_793del
ENST00000265384.11:c.766_769del ENSP00000265384.7:p.Ala256ThrfsTer?
ENST00000348208.8:c.766_769del ENSP00000345893.4:p.Ala256ThrfsTer?
ENST00000377245.8:c.766_769del ENSP00000366453.4:p.Ala256ThrfsTer?
ENST00000453658.6:c.697_700del ENSP00000392178.2:p.Ala233ThrfsTer?
ENST00000535702.5:c.778_781del ENSP00000442090.1:p.Ala260ThrfsTer?
ENST00000539225.1:c.859_862del ENSP00000438262.1:p.Ala287ThrfsTer?
NM_001170414.2:c.697_700del NP_001163885.1:p.Ala233ThrfsTer?
NM_001170415.1:c.778_781del NP_001163886.1:p.Ala260ThrfsTer?
NM_001170416.1:c.859_862del NP_001163887.1:p.Ala287ThrfsTer?
NM_001170630.1:c.766_769del NP_001164101.1:p.Ala256ThrfsTer?
NM_004817.3:c.766_769del NP_004808.2:p.Ala256ThrfsTer?
NM_201629.3:c.766_769del NP_963923.1:p.Ala256ThrfsTer?
XM_005252314.1:c.778_781del XP_005252371.1:p.Ala260ThrfsTer?
XM_006717324.2:c.760_763del XP_006717387.1:p.Ala254ThrfsTer?
XM_011519204.1:c.697_700del XP_011517506.1:p.Ala233ThrfsTer?
XM_011519205.1:c.697_700del XP_011517507.1:p.Ala233ThrfsTer?
XM_011519206.1:c.697_700del XP_011517508.1:p.Ala233ThrfsTer?
XM_011519207.1:c.697_700del XP_011517509.1:p.Ala233ThrfsTer?
XM_011519208.1:c.697_700del XP_011517510.1:p.Ala233ThrfsTer?
XM_011519209.1:c.697_700del XP_011517511.1:p.Ala233ThrfsTer?
NM_004817.4:c.766_769del MANE Select NP_004808.2:p.Ala256ThrfsTer?
XM_005252314.2:c.778_781del XP_005252371.1:p.Ala260ThrfsTer?
XM_011519206.2:c.697_700del XP_011517508.1:p.Ala233ThrfsTer?
XM_011519207.2:c.697_700del XP_011517509.1:p.Ala233ThrfsTer?
XM_011519208.2:c.697_700del XP_011517510.1:p.Ala233ThrfsTer?
XM_011519209.2:c.697_700del XP_011517511.1:p.Ala233ThrfsTer?
XM_017015327.2:c.766_769del XP_016870816.1:p.Ala256ThrfsTer?
XM_017015328.1:c.778_781del XP_016870817.1:p.Ala260ThrfsTer?
NM_001170416.2:c.859_862del NP_001163887.1:p.Ala287ThrfsTer?
NM_001369870.1:c.697_700del NP_001356799.1:p.Ala233ThrfsTer?
NM_001369871.1:c.697_700del NP_001356800.1:p.Ala233ThrfsTer?
NM_001369872.1:c.766_769del NP_001356801.1:p.Ala256ThrfsTer?
NM_001369873.1:c.766_769del NP_001356802.1:p.Ala256ThrfsTer?
NM_001369874.1:c.778_781del NP_001356803.1:p.Ala260ThrfsTer?
NM_001369875.1:c.778_781del NP_001356804.1:p.Ala260ThrfsTer?