Canonical Allele Identifier: CA411446849
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710478T>C , CM000684.2:g.37710478T>C GRCh38
NC_000022.10:g.38106485T>C , CM000684.1:g.38106485T>C GRCh37
NC_000022.9:g.36436431T>C NCBI36
NG_012857.1:g.18491T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.166T>C MANE Select ENSP00000496394.1:p.Cys56Arg
ENST00000344404.10:c.166T>C ENSP00000340312.6:p.Cys56Arg
ENST00000406386.7:c.166T>C ENSP00000384312.3:p.Cys56Arg
ENST00000455236.4:c.1123T>C ENSP00000477208.1:n.1123T>C
ENST00000492485.5:n.302T>C
NM_001039141.2:c.166T>C NP_001034230.1:p.Cys56Arg
NM_001039141.3:c.166T>C MANE Select NP_001034230.1:p.Cys56Arg