Canonical Allele Identifier: CA411447662
Gene: TRIOBP HGNC NCBI

Linked Data

COSMIC: COSM726363

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713210G>C , CM000684.2:g.37713210G>C GRCh38
NC_000022.10:g.38109217G>C , CM000684.1:g.38109217G>C GRCh37
NC_000022.9:g.36439163G>C NCBI36
NG_012857.1:g.21223G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.255G>C MANE Select ENSP00000496394.1:p.Arg85Ser
ENST00000344404.10:c.255-2553G>C ENSP00000340312.6:n.255-2553G>C
ENST00000406386.7:c.255G>C ENSP00000384312.3:p.Arg85Ser
ENST00000455236.4:c.1212G>C ENSP00000477208.1:n.1212G>C
ENST00000492485.5:n.391-2553G>C
NM_001039141.2:c.255G>C NP_001034230.1:p.Arg85Ser
NM_001039141.3:c.255G>C MANE Select NP_001034230.1:p.Arg85Ser