Canonical Allele Identifier: CA2404479974
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37723911_37723989delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG , CM000684.2:g.37723911_37723989delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG GRCh38
NC_000022.10:g.38119918_38119996delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG , CM000684.1:g.38119918_38119996delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG GRCh37
NC_000022.9:g.36449864_36449942delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG NCBI36
NG_012857.1:g.31924_32002delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.1355_1433delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG MANE Select ENSP00000496394.1:p.Thr452=
ENST00000344404.10:c.*838_*916delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG ENSP00000340312.6:n.*838_*916delinsCAACAT...
ENST00000406386.7:c.1355_1433delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG ENSP00000384312.3:p.Thr452=
ENST00000455236.4:c.2312_2390delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG ENSP00000477208.1:n.2312_2390delinsCAACAT...
ENST00000492485.5:n.1289_1367delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG
NM_001039141.2:c.1355_1433delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG NP_001034230.1:p.Thr452=
NM_001039141.3:c.1355_1433delinsCAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAG MANE Select NP_001034230.1:p.Thr452=