Canonical Allele Identifier: CA509324396

Gene: TRIB3

Linked Data

• MyVariant Identifiers: chr20:g.368831A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388187A>T , CM000682.2:g.388187A>T	GRCh38
NC_000020.10:g.368831A>T , CM000682.1:g.368831A>T	GRCh37
NC_000020.9:g.316831A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217233.9:c.177A>T MANE Select	ENSP00000217233.3:p.Ala59=
ENST00000217233.8:c.177A>T	ENSP00000217233.3:p.Ala59=
ENST00000217233.7:c.177A>T	ENSP00000217233.3:p.Ala59=
ENST00000422053.3:c.258A>T	ENSP00000415416.2:p.Ala86=
ENST00000449710.5:c.177A>T	ENSP00000391873.1:p.Ala59=
ENST00000615226.4:c.177A>T	ENSP00000478194.1:p.Ala59=
NM_001301188.1:c.177A>T	NP_001288117.1:p.Ala59=
NM_001301190.1:c.177A>T	NP_001288119.1:p.Ala59=
NM_001301193.1:c.177A>T	NP_001288122.1:p.Ala59=
NM_001301196.1:c.177A>T	NP_001288125.1:p.Ala59=
NM_001301201.1:c.258A>T	NP_001288130.1:p.Ala86=
NM_021158.4:c.177A>T	NP_066981.2:p.Ala59=
XM_017027989.2:c.258A>T	XP_016883478.1:p.Ala86=
NM_021158.5:c.177A>T MANE Select	NP_066981.2:p.Ala59=