Canonical Allele Identifier: CA2818916998
Gene: TRIOBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733403dup , CM000684.2:g.37733403dup GRCh38
NC_000022.10:g.38129410dup , CM000684.1:g.38129410dup GRCh37
NC_000022.9:g.36459356dup NCBI36
NG_012857.1:g.41416dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4053dup MANE Select ENSP00000496394.1:p.Ser1352GlnfsTer29
ENST00000344404.10:c.*3536dup ENSP00000340312.6:n.*3536dup
ENST00000406386.7:c.4053dup ENSP00000384312.3:p.Ser1352GlnfsTer29
NM_001039141.2:c.4053dup NP_001034230.1:p.Ser1352GlnfsTer29
XM_011530646.1:c.512-3040dup XP_011528948.1:n.512-3040dup
NM_001039141.3:c.4053dup MANE Select NP_001034230.1:p.Ser1352GlnfsTer29
Search 100 bp 5'
Search 100 bp 3'