Canonical Allele Identifier: CA411510335
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38164141G>C (hg19) chr22:g.37768134G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768134G>C , CM000684.2:g.37768134G>C GRCh38
NC_000022.10:g.38164141G>C , CM000684.1:g.38164141G>C GRCh37
NC_000022.9:g.36494087G>C NCBI36
NG_012857.1:g.76147G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6533G>C MANE Select ENSP00000496394.1:p.Arg2178Pro
ENST00000344404.10:c.*6016G>C ENSP00000340312.6:n.*6016G>C
ENST00000403663.6:c.1394G>C ENSP00000386026.2:p.Arg465Pro
ENST00000406386.7:c.6533G>C ENSP00000384312.3:p.Arg2178Pro
NM_001039141.2:c.6533G>C NP_001034230.1:p.Arg2178Pro
NM_007032.5:c.1394G>C NP_008963.3:p.Arg465Pro
NM_001039141.3:c.6533G>C MANE Select NP_001034230.1:p.Arg2178Pro
Search 100 bp 5'
Search 100 bp 3'