Canonical Allele Identifier: CA411449826
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715770A>T , CM000684.2:g.37715770A>T GRCh38
NC_000022.10:g.38111777A>T , CM000684.1:g.38111777A>T GRCh37
NC_000022.9:g.36441723A>T NCBI36
NG_012857.1:g.23783A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.464A>T MANE Select ENSP00000496394.1:p.Asp155Val
ENST00000344404.10:c.262A>T ENSP00000340312.6:p.Thr88Ser
ENST00000406386.7:c.464A>T ENSP00000384312.3:p.Asp155Val
ENST00000455236.4:c.1421A>T ENSP00000477208.1:n.1421A>T
ENST00000492485.5:n.398A>T
NM_001039141.2:c.464A>T NP_001034230.1:p.Asp155Val
NM_001039141.3:c.464A>T MANE Select NP_001034230.1:p.Asp155Val