Canonical Allele Identifier: CA2843661138
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715985del , CM000684.2:g.37715985del GRCh38
NC_000022.10:g.38111992del , CM000684.1:g.38111992del GRCh37
NC_000022.9:g.36441938del NCBI36
NG_012857.1:g.23998del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.628+51del MANE Select ENSP00000496394.1:n.628+51del
ENST00000344404.10:c.*111+51del ENSP00000340312.6:n.*111+51del
ENST00000406386.7:c.628+51del ENSP00000384312.3:n.628+51del
ENST00000455236.4:c.1585+51del ENSP00000477208.1:n.1585+51del
ENST00000492485.5:n.562+51del
NM_001039141.2:c.628+51del NP_001034230.1:n.628+51del
NM_001039141.3:c.628+51del MANE Select NP_001034230.1:n.628+51del