Canonical Allele Identifier: CA9722513
Gene: TRIB3 HGNC NCBI

Linked Data

dbSNP Id: rs745734359
gnomAD v2: 20-368783-GC-G
gnomAD v3: 20-388139-GC-G
gnomAD v4: 20-388139-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.388145del , CM000682.2:g.388145del GRCh38
NC_000020.10:g.368789del , CM000682.1:g.368789del GRCh37
NC_000020.9:g.316789del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000217233.9:c.135del MANE Select ENSP00000217233.3:p.Cys46AlafsTer5
ENST00000217233.8:c.135del ENSP00000217233.3:p.Cys46AlafsTer5
ENST00000217233.7:c.135del ENSP00000217233.3:p.Cys46AlafsTer5
ENST00000422053.3:c.216del ENSP00000415416.2:p.Cys73AlafsTer5
ENST00000449710.5:c.135del ENSP00000391873.1:p.Cys46AlafsTer5
ENST00000615226.4:c.135del ENSP00000478194.1:p.Cys46AlafsTer5
NM_001301188.1:c.135del NP_001288117.1:p.Cys46AlafsTer5
NM_001301190.1:c.135del NP_001288119.1:p.Cys46AlafsTer5
NM_001301193.1:c.135del NP_001288122.1:p.Cys46AlafsTer5
NM_001301196.1:c.135del NP_001288125.1:p.Cys46AlafsTer5
NM_001301201.1:c.216del NP_001288130.1:p.Cys73AlafsTer5
NM_021158.4:c.135del NP_066981.2:p.Cys46AlafsTer5
XM_017027989.2:c.216del XP_016883478.1:p.Cys73AlafsTer5
NM_021158.5:c.135del MANE Select NP_066981.2:p.Cys46AlafsTer5