Canonical Allele Identifier: CA514524846
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38106448T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710441T>A , CM000684.2:g.37710441T>A GRCh38
NC_000022.10:g.38106448T>A , CM000684.1:g.38106448T>A GRCh37
NC_000022.9:g.36436394T>A NCBI36
NG_012857.1:g.18454T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.129T>A MANE Select ENSP00000496394.1:p.Pro43=
ENST00000344404.10:c.129T>A ENSP00000340312.6:p.Pro43=
ENST00000406386.7:c.129T>A ENSP00000384312.3:p.Pro43=
ENST00000455236.4:c.1086T>A ENSP00000477208.1:n.1086T>A
ENST00000492485.5:n.265T>A
NM_001039141.2:c.129T>A NP_001034230.1:p.Pro43=
NM_001039141.3:c.129T>A MANE Select NP_001034230.1:p.Pro43=