Canonical Allele Identifier: CA407922309

Gene: TRIB3

Linked Data

• gnomAD v4: 20-388102-T-C
• MyVariant Identifiers: chr20:g.368746T>C (hg19) ; chr20:g.388102T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388102T>C , CM000682.2:g.388102T>C	GRCh38
NC_000020.10:g.368746T>C , CM000682.1:g.368746T>C	GRCh37
NC_000020.9:g.316746T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217233.9:c.92T>C MANE Select	ENSP00000217233.3:p.Val31Ala
ENST00000217233.8:c.92T>C	ENSP00000217233.3:p.Val31Ala
ENST00000217233.7:c.92T>C	ENSP00000217233.3:p.Val31Ala
ENST00000422053.3:c.173T>C	ENSP00000415416.2:p.Val58Ala
ENST00000449710.5:c.92T>C	ENSP00000391873.1:p.Val31Ala
ENST00000615226.4:c.92T>C	ENSP00000478194.1:p.Val31Ala
NM_001301188.1:c.92T>C	NP_001288117.1:p.Val31Ala
NM_001301190.1:c.92T>C	NP_001288119.1:p.Val31Ala
NM_001301193.1:c.92T>C	NP_001288122.1:p.Val31Ala
NM_001301196.1:c.92T>C	NP_001288125.1:p.Val31Ala
NM_001301201.1:c.173T>C	NP_001288130.1:p.Val58Ala
NM_021158.4:c.92T>C	NP_066981.2:p.Val31Ala
XM_017027989.2:c.173T>C	XP_016883478.1:p.Val58Ala
NM_021158.5:c.92T>C MANE Select	NP_066981.2:p.Val31Ala