Canonical Allele Identifier: CA9722523

Gene: TRIB3

Linked Data

• dbSNP Id: rs755979873
• ExAC: 20:368802 CT / C
• gnomAD v2: 20-368802-CT-C
• gnomAD v4: 20-388158-CT-C
• MyVariant Identifiers: chr20:g.368803del (hg19) ; chr20:g.388159del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388159del , CM000682.2:g.388159del	GRCh38
NC_000020.10:g.368803del , CM000682.1:g.368803del	GRCh37
NC_000020.9:g.316803del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217233.9:c.149del MANE Select	ENSP00000217233.3:p.Leu50ArgfsTer?
ENST00000217233.8:c.149del	ENSP00000217233.3:p.Leu50ArgfsTer?
ENST00000217233.7:c.149del	ENSP00000217233.3:p.Leu50ArgfsTer?
ENST00000422053.3:c.230del	ENSP00000415416.2:p.Leu77ArgfsTer?
ENST00000449710.5:c.149del	ENSP00000391873.1:p.Leu50ArgfsTer?
ENST00000615226.4:c.149del	ENSP00000478194.1:p.Leu50ArgfsTer?
NM_001301188.1:c.149del	NP_001288117.1:p.Leu50ArgfsTer?
NM_001301190.1:c.149del	NP_001288119.1:p.Leu50ArgfsTer?
NM_001301193.1:c.149del	NP_001288122.1:p.Leu50ArgfsTer?
NM_001301196.1:c.149del	NP_001288125.1:p.Leu50ArgfsTer?
NM_001301201.1:c.230del	NP_001288130.1:p.Leu77ArgfsTer?
NM_021158.4:c.149del	NP_066981.2:p.Leu50ArgfsTer?
XM_017027989.2:c.230del	XP_016883478.1:p.Leu77ArgfsTer?
NM_021158.5:c.149del MANE Select	NP_066981.2:p.Leu50ArgfsTer?