Canonical Allele Identifier: CA2656568668
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733154_37733155del , CM000684.2:g.37733154_37733155del GRCh38
NC_000022.10:g.38129161_38129162del , CM000684.1:g.38129161_38129162del GRCh37
NC_000022.9:g.36459107_36459108del NCBI36
NG_012857.1:g.41167_41168del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-144_3948-143del MANE Select ENSP00000496394.1:n.3948-144_3948-143del
ENST00000344404.10:c.*3431-144_*3431-143del ENSP00000340312.6:n.*3431-144_*3431-143del
ENST00000406386.7:c.3948-144_3948-143del ENSP00000384312.3:n.3948-144_3948-143del
NM_001039141.2:c.3948-144_3948-143del NP_001034230.1:n.3948-144_3948-143del
XM_011530646.1:c.512-2793_512-2792del XP_011528948.1:n.512-2793_512-2792del
NM_001039141.3:c.3948-144_3948-143del MANE Select NP_001034230.1:n.3948-144_3948-143del