Canonical Allele Identifier: CA2404474638
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713462_37713465delinsTGCA , CM000684.2:g.37713462_37713465delinsTGCA GRCh38
NC_000022.10:g.38109469_38109472delinsTGCA , CM000684.1:g.38109469_38109472delinsTGCA GRCh37
NC_000022.9:g.36439415_36439418delinsTGCA NCBI36
NG_012857.1:g.21475_21478delinsTGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.456+51_456+54delinsTGCA MANE Select ENSP00000496394.1:n.456+51_456+54delinsTGCA
ENST00000344404.10:c.255-2301_255-2298delinsTGCA ENSP00000340312.6:n.255-2301_255-2298delinsTGCA
ENST00000406386.7:c.456+51_456+54delinsTGCA ENSP00000384312.3:n.456+51_456+54delinsTGCA
ENST00000455236.4:c.1413+51_1413+54delinsTGCA ENSP00000477208.1:n.1413+51_1413+54delinsTGCA
ENST00000492485.5:n.391-2301_391-2298delinsTGCA
NM_001039141.2:c.456+51_456+54delinsTGCA NP_001034230.1:n.456+51_456+54delinsTGCA
NM_001039141.3:c.456+51_456+54delinsTGCA MANE Select NP_001034230.1:n.456+51_456+54delinsTGCA