Canonical Allele Identifier: CA2590275052
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs2145819351
gnomAD v3: 22-37710647-GC-G
gnomAD v4: 22-37710647-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710648del , CM000684.2:g.37710648del GRCh38
NC_000022.10:g.38106655del , CM000684.1:g.38106655del GRCh37
NC_000022.9:g.36436601del NCBI36
NG_012857.1:g.18661del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.254+82del MANE Select ENSP00000496394.1:n.254+82del
ENST00000344404.10:c.254+82del ENSP00000340312.6:n.254+82del
ENST00000406386.7:c.254+82del ENSP00000384312.3:n.254+82del
ENST00000455236.4:c.1211+82del ENSP00000477208.1:n.1211+82del
ENST00000492485.5:n.390+82del
NM_001039141.2:c.254+82del NP_001034230.1:n.254+82del
NM_001039141.3:c.254+82del MANE Select NP_001034230.1:n.254+82del
Search 100 bp 5'
Search 100 bp 3'