Canonical Allele Identifier: CA407922670

Gene: TRIB3

Linked Data

• COSMIC: COSM1026634
• MyVariant Identifiers: chr20:g.368818C>T (hg19) ; chr20:g.388174C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000217233.9:c.164C>T MANE Select	ENSP00000217233.3:p.Ala55Val
ENST00000217233.8:c.164C>T	ENSP00000217233.3:p.Ala55Val
ENST00000217233.7:c.164C>T	ENSP00000217233.3:p.Ala55Val
ENST00000422053.3:c.245C>T	ENSP00000415416.2:p.Ala82Val
ENST00000449710.5:c.164C>T	ENSP00000391873.1:p.Ala55Val
ENST00000615226.4:c.164C>T	ENSP00000478194.1:p.Ala55Val
NM_001301188.1:c.164C>T	NP_001288117.1:p.Ala55Val
NM_001301190.1:c.164C>T	NP_001288119.1:p.Ala55Val
NM_001301193.1:c.164C>T	NP_001288122.1:p.Ala55Val
NM_001301196.1:c.164C>T	NP_001288125.1:p.Ala55Val
NM_001301201.1:c.245C>T	NP_001288130.1:p.Ala82Val
NM_021158.4:c.164C>T	NP_066981.2:p.Ala55Val
XM_017027989.2:c.245C>T	XP_016883478.1:p.Ala82Val
NM_021158.5:c.164C>T MANE Select	NP_066981.2:p.Ala55Val