Canonical Allele Identifier: CA411447189
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs750657153

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710566G>A , CM000684.2:g.37710566G>A GRCh38
NC_000022.10:g.38106573G>A , CM000684.1:g.38106573G>A GRCh37
NC_000022.9:g.36436519G>A NCBI36
NG_012857.1:g.18579G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.254G>A MANE Select ENSP00000496394.1:p.Arg85Lys
ENST00000344404.10:c.254G>A ENSP00000340312.6:p.Arg85Lys
ENST00000406386.7:c.254G>A ENSP00000384312.3:p.Arg85Lys
ENST00000455236.4:c.1211G>A ENSP00000477208.1:n.1211G>A
ENST00000492485.5:n.390G>A
NM_001039141.2:c.254G>A NP_001034230.1:p.Arg85Lys
NM_001039141.3:c.254G>A MANE Select NP_001034230.1:p.Arg85Lys