Canonical Allele Identifier: CA2345171122
Gene: TRIB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.388125C= , CM000682.2:g.388125C= GRCh38
NC_000020.10:g.368769C= , CM000682.1:g.368769C= GRCh37
NC_000020.9:g.316769C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000217233.9:c.115C= MANE Select ENSP00000217233.3:p.Pro39=
ENST00000217233.8:c.115C= ENSP00000217233.3:p.Pro39=
ENST00000217233.7:c.115C= ENSP00000217233.3:p.Pro39=
ENST00000422053.3:c.196C= ENSP00000415416.2:p.Pro66=
ENST00000449710.5:c.115C= ENSP00000391873.1:p.Pro39=
ENST00000615226.4:c.115C= ENSP00000478194.1:p.Pro39=
NM_001301188.1:c.115C= NP_001288117.1:p.Pro39=
NM_001301190.1:c.115C= NP_001288119.1:p.Pro39=
NM_001301193.1:c.115C= NP_001288122.1:p.Pro39=
NM_001301196.1:c.115C= NP_001288125.1:p.Pro39=
NM_001301201.1:c.196C= NP_001288130.1:p.Pro66=
NM_021158.4:c.115C= NP_066981.2:p.Pro39=
XM_017027989.2:c.196C= XP_016883478.1:p.Pro66=
NM_021158.5:c.115C= MANE Select NP_066981.2:p.Pro39=