Canonical Allele Identifier: CA2843661123
Gene: TRIOBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715705T>A , CM000684.2:g.37715705T>A GRCh38
NC_000022.10:g.38111712T>A , CM000684.1:g.38111712T>A GRCh37
NC_000022.9:g.36441658T>A NCBI36
NG_012857.1:g.23718T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.457-58T>A MANE Select ENSP00000496394.1:n.457-58T>A
ENST00000344404.10:c.255-58T>A ENSP00000340312.6:n.255-58T>A
ENST00000406386.7:c.457-58T>A ENSP00000384312.3:n.457-58T>A
ENST00000455236.4:c.1414-58T>A ENSP00000477208.1:n.1414-58T>A
ENST00000492485.5:n.391-58T>A
NM_001039141.2:c.457-58T>A NP_001034230.1:n.457-58T>A
NM_001039141.3:c.457-58T>A MANE Select NP_001034230.1:n.457-58T>A
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