Canonical Allele Identifier: CA411446984
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710509C>A , CM000684.2:g.37710509C>A GRCh38
NC_000022.10:g.38106516C>A , CM000684.1:g.38106516C>A GRCh37
NC_000022.9:g.36436462C>A NCBI36
NG_012857.1:g.18522C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.197C>A MANE Select ENSP00000496394.1:p.Ala66Asp
ENST00000344404.10:c.197C>A ENSP00000340312.6:p.Ala66Asp
ENST00000406386.7:c.197C>A ENSP00000384312.3:p.Ala66Asp
ENST00000455236.4:c.1154C>A ENSP00000477208.1:n.1154C>A
ENST00000492485.5:n.333C>A
NM_001039141.2:c.197C>A NP_001034230.1:p.Ala66Asp
NM_001039141.3:c.197C>A MANE Select NP_001034230.1:p.Ala66Asp