Canonical Allele Identifier: CA251858
Gene: TRIOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1495
dbSNP Id: rs118204031

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37725905C>T , CM000684.2:g.37725905C>T GRCh38
NC_000022.10:g.38121912C>T , CM000684.1:g.38121912C>T GRCh37
NC_000022.9:g.36451858C>T NCBI36
NG_012857.1:g.33918C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.3349C>T MANE Select ENSP00000496394.1:p.Arg1117Ter
ENST00000344404.10:c.*2832C>T ENSP00000340312.6:n.*2832C>T
ENST00000406386.7:c.3349C>T ENSP00000384312.3:p.Arg1117Ter
ENST00000455236.4:c.4306C>T ENSP00000477208.1:n.4306C>T
ENST00000492485.5:n.3283C>T
NM_001039141.2:c.3349C>T NP_001034230.1:p.Arg1117Ter
NM_001039141.3:c.3349C>T MANE Select NP_001034230.1:p.Arg1117Ter