Canonical Allele Identifier: CA2577710539
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713510_37713511del , CM000684.2:g.37713510_37713511del GRCh38
NC_000022.10:g.38109517_38109518del , CM000684.1:g.38109517_38109518del GRCh37
NC_000022.9:g.36439463_36439464del NCBI36
NG_012857.1:g.21523_21524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.456+99_456+100del MANE Select ENSP00000496394.1:n.456+99_456+100del
ENST00000344404.10:c.255-2253_255-2252del ENSP00000340312.6:n.255-2253_255-2252del
ENST00000406386.7:c.456+99_456+100del ENSP00000384312.3:n.456+99_456+100del
ENST00000455236.4:c.1413+99_1413+100del ENSP00000477208.1:n.1413+99_1413+100del
ENST00000492485.5:n.391-2253_391-2252del
NM_001039141.2:c.456+99_456+100del NP_001034230.1:n.456+99_456+100del
NM_001039141.3:c.456+99_456+100del MANE Select NP_001034230.1:n.456+99_456+100del