Canonical Allele Identifier: CA2345171129

Gene: TRIB3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.388139_388140delinsGC , CM000682.2:g.388139_388140delinsGC	GRCh38
NC_000020.10:g.368783_368784delinsGC , CM000682.1:g.368783_368784delinsGC	GRCh37
NC_000020.9:g.316783_316784delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217233.9:c.129_130delinsGC MANE Select	ENSP00000217233.3:p.Leu43=
ENST00000217233.8:c.129_130delinsGC	ENSP00000217233.3:p.Leu43=
ENST00000217233.7:c.129_130delinsGC	ENSP00000217233.3:p.Leu43=
ENST00000422053.3:c.210_211delinsGC	ENSP00000415416.2:p.Leu70=
ENST00000449710.5:c.129_130delinsGC	ENSP00000391873.1:p.Leu43=
ENST00000615226.4:c.129_130delinsGC	ENSP00000478194.1:p.Leu43=
NM_001301188.1:c.129_130delinsGC	NP_001288117.1:p.Leu43=
NM_001301190.1:c.129_130delinsGC	NP_001288119.1:p.Leu43=
NM_001301193.1:c.129_130delinsGC	NP_001288122.1:p.Leu43=
NM_001301196.1:c.129_130delinsGC	NP_001288125.1:p.Leu43=
NM_001301201.1:c.210_211delinsGC	NP_001288130.1:p.Leu70=
NM_021158.4:c.129_130delinsGC	NP_066981.2:p.Leu43=
XM_017027989.2:c.210_211delinsGC	XP_016883478.1:p.Leu70=
NM_021158.5:c.129_130delinsGC MANE Select	NP_066981.2:p.Leu43=