Canonical Allele Identifier: CA2345171149
Gene: TRIB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.388179G= , CM000682.2:g.388179G= GRCh38
NC_000020.10:g.368823G= , CM000682.1:g.368823G= GRCh37
NC_000020.9:g.316823G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000217233.9:c.169G= MANE Select ENSP00000217233.3:p.Asp57=
ENST00000217233.8:c.169G= ENSP00000217233.3:p.Asp57=
ENST00000217233.7:c.169G= ENSP00000217233.3:p.Asp57=
ENST00000422053.3:c.250G= ENSP00000415416.2:p.Asp84=
ENST00000449710.5:c.169G= ENSP00000391873.1:p.Asp57=
ENST00000615226.4:c.169G= ENSP00000478194.1:p.Asp57=
NM_001301188.1:c.169G= NP_001288117.1:p.Asp57=
NM_001301190.1:c.169G= NP_001288119.1:p.Asp57=
NM_001301193.1:c.169G= NP_001288122.1:p.Asp57=
NM_001301196.1:c.169G= NP_001288125.1:p.Asp57=
NM_001301201.1:c.250G= NP_001288130.1:p.Asp84=
NM_021158.4:c.169G= NP_066981.2:p.Asp57=
XM_017027989.2:c.250G= XP_016883478.1:p.Asp84=
NM_021158.5:c.169G= MANE Select NP_066981.2:p.Asp57=