Canonical Allele Identifier: CA2577710556
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715944_37715946del , CM000684.2:g.37715944_37715946del GRCh38
NC_000022.10:g.38111951_38111953del , CM000684.1:g.38111951_38111953del GRCh37
NC_000022.9:g.36441897_36441899del NCBI36
NG_012857.1:g.23957_23959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.628+10_628+12del MANE Select ENSP00000496394.1:n.628+10_628+12del
ENST00000344404.10:c.*111+10_*111+12del ENSP00000340312.6:n.*111+10_*111+12del
ENST00000406386.7:c.628+10_628+12del ENSP00000384312.3:n.628+10_628+12del
ENST00000455236.4:c.1585+10_1585+12del ENSP00000477208.1:n.1585+10_1585+12del
ENST00000492485.5:n.562+10_562+12del
NM_001039141.2:c.628+10_628+12del NP_001034230.1:n.628+10_628+12del
NM_001039141.3:c.628+10_628+12del MANE Select NP_001034230.1:n.628+10_628+12del