Canonical Allele Identifier: CA310649557

Gene: TRIB3

Linked Data

• dbSNP Id: rs767505682
• gnomAD v2: 20-368915-C-CT
• gnomAD v3: 20-388271-C-CT
• gnomAD v4: 20-388271-C-CT
• MyVariant Identifiers: chr20:g.368915_368916insT (hg19) ; chr20:g.388271_388272insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388272dup , CM000682.2:g.388272dup	GRCh38
NC_000020.10:g.368916dup , CM000682.1:g.368916dup	GRCh37
NC_000020.9:g.316916dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000217233.9:c.262dup MANE Select	ENSP00000217233.3:p.Cys88LeufsTer6
ENST00000217233.8:c.262dup	ENSP00000217233.3:p.Cys88LeufsTer6
ENST00000217233.7:c.262dup	ENSP00000217233.3:p.Cys88LeufsTer6
ENST00000422053.3:c.343dup	ENSP00000415416.2:p.Cys115LeufsTer6
ENST00000449710.5:c.262dup	ENSP00000391873.1:p.Cys88LeufsTer6
ENST00000615226.4:c.262dup	ENSP00000478194.1:p.Cys88LeufsTer6
NM_001301188.1:c.262dup	NP_001288117.1:p.Cys88LeufsTer6
NM_001301190.1:c.262dup	NP_001288119.1:p.Cys88LeufsTer6
NM_001301193.1:c.262dup	NP_001288122.1:p.Cys88LeufsTer6
NM_001301196.1:c.262dup	NP_001288125.1:p.Cys88LeufsTer6
NM_001301201.1:c.343dup	NP_001288130.1:p.Cys115LeufsTer6
NM_021158.4:c.262dup	NP_066981.2:p.Cys88LeufsTer6
XM_017027989.2:c.343dup	XP_016883478.1:p.Cys115LeufsTer6
NM_021158.5:c.262dup MANE Select	NP_066981.2:p.Cys88LeufsTer6