Canonical Allele Identifier: CA514525170
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38109301C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713294C>A , CM000684.2:g.37713294C>A GRCh38
NC_000022.10:g.38109301C>A , CM000684.1:g.38109301C>A GRCh37
NC_000022.9:g.36439247C>A NCBI36
NG_012857.1:g.21307C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.339C>A MANE Select ENSP00000496394.1:p.Pro113=
ENST00000344404.10:c.255-2469C>A ENSP00000340312.6:n.255-2469C>A
ENST00000406386.7:c.339C>A ENSP00000384312.3:p.Pro113=
ENST00000455236.4:c.1296C>A ENSP00000477208.1:n.1296C>A
ENST00000492485.5:n.391-2469C>A
NM_001039141.2:c.339C>A NP_001034230.1:p.Pro113=
NM_001039141.3:c.339C>A MANE Select NP_001034230.1:p.Pro113=
Search 100 bp 5'
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