Canonical Allele Identifier: CA2656568714
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733165_37733168del , CM000684.2:g.37733165_37733168del GRCh38
NC_000022.10:g.38129172_38129175del , CM000684.1:g.38129172_38129175del GRCh37
NC_000022.9:g.36459118_36459121del NCBI36
NG_012857.1:g.41178_41181del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-133_3948-130del MANE Select ENSP00000496394.1:n.3948-133_3948-130del
ENST00000344404.10:c.*3431-133_*3431-130del ENSP00000340312.6:n.*3431-133_*3431-130del
ENST00000406386.7:c.3948-133_3948-130del ENSP00000384312.3:n.3948-133_3948-130del
NM_001039141.2:c.3948-133_3948-130del NP_001034230.1:n.3948-133_3948-130del
XM_011530646.1:c.512-2808_512-2805del XP_011528948.1:n.512-2808_512-2805del
NM_001039141.3:c.3948-133_3948-130del MANE Select NP_001034230.1:n.3948-133_3948-130del