Canonical Allele Identifier: CA411447152
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710560C>G , CM000684.2:g.37710560C>G GRCh38
NC_000022.10:g.38106567C>G , CM000684.1:g.38106567C>G GRCh37
NC_000022.9:g.36436513C>G NCBI36
NG_012857.1:g.18573C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.248C>G MANE Select ENSP00000496394.1:p.Pro83Arg
ENST00000344404.10:c.248C>G ENSP00000340312.6:p.Pro83Arg
ENST00000406386.7:c.248C>G ENSP00000384312.3:p.Pro83Arg
ENST00000455236.4:c.1205C>G ENSP00000477208.1:n.1205C>G
ENST00000492485.5:n.384C>G
NM_001039141.2:c.248C>G NP_001034230.1:p.Pro83Arg
NM_001039141.3:c.248C>G MANE Select NP_001034230.1:p.Pro83Arg