Canonical Allele Identifier: CA411450477
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111875C>A (hg19) chr22:g.37715868C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715868C>A , CM000684.2:g.37715868C>A GRCh38
NC_000022.10:g.38111875C>A , CM000684.1:g.38111875C>A GRCh37
NC_000022.9:g.36441821C>A NCBI36
NG_012857.1:g.23881C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.562C>A MANE Select ENSP00000496394.1:p.Gln188Lys
ENST00000344404.10:c.*45C>A ENSP00000340312.6:n.*45C>A
ENST00000406386.7:c.562C>A ENSP00000384312.3:p.Gln188Lys
ENST00000455236.4:c.1519C>A ENSP00000477208.1:n.1519C>A
ENST00000492485.5:n.496C>A
NM_001039141.2:c.562C>A NP_001034230.1:p.Gln188Lys
NM_001039141.3:c.562C>A MANE Select NP_001034230.1:p.Gln188Lys
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