Canonical Allele Identifier: CA407922661

Gene: TRIB3

Linked Data

• MyVariant Identifiers: chr20:g.368818C>A (hg19) ; chr20:g.388174C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388174C>A , CM000682.2:g.388174C>A	GRCh38
NC_000020.10:g.368818C>A , CM000682.1:g.368818C>A	GRCh37
NC_000020.9:g.316818C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000217233.9:c.164C>A MANE Select	ENSP00000217233.3:p.Ala55Asp
ENST00000217233.8:c.164C>A	ENSP00000217233.3:p.Ala55Asp
ENST00000217233.7:c.164C>A	ENSP00000217233.3:p.Ala55Asp
ENST00000422053.3:c.245C>A	ENSP00000415416.2:p.Ala82Asp
ENST00000449710.5:c.164C>A	ENSP00000391873.1:p.Ala55Asp
ENST00000615226.4:c.164C>A	ENSP00000478194.1:p.Ala55Asp
NM_001301188.1:c.164C>A	NP_001288117.1:p.Ala55Asp
NM_001301190.1:c.164C>A	NP_001288119.1:p.Ala55Asp
NM_001301193.1:c.164C>A	NP_001288122.1:p.Ala55Asp
NM_001301196.1:c.164C>A	NP_001288125.1:p.Ala55Asp
NM_001301201.1:c.245C>A	NP_001288130.1:p.Ala82Asp
NM_021158.4:c.164C>A	NP_066981.2:p.Ala55Asp
XM_017027989.2:c.245C>A	XP_016883478.1:p.Ala82Asp
NM_021158.5:c.164C>A MANE Select	NP_066981.2:p.Ala55Asp