Canonical Allele Identifier: CA514525392
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111808C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715801C>A , CM000684.2:g.37715801C>A GRCh38
NC_000022.10:g.38111808C>A , CM000684.1:g.38111808C>A GRCh37
NC_000022.9:g.36441754C>A NCBI36
NG_012857.1:g.23814C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.495C>A MANE Select ENSP00000496394.1:p.Pro165=
ENST00000344404.10:c.293C>A ENSP00000340312.6:p.Pro98Gln
ENST00000406386.7:c.495C>A ENSP00000384312.3:p.Pro165=
ENST00000455236.4:c.1452C>A ENSP00000477208.1:n.1452C>A
ENST00000492485.5:n.429C>A
NM_001039141.2:c.495C>A NP_001034230.1:p.Pro165=
NM_001039141.3:c.495C>A MANE Select NP_001034230.1:p.Pro165=