Canonical Allele Identifier: CA411487241
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38129354C>G (hg19) chr22:g.37733347C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733347C>G , CM000684.2:g.37733347C>G GRCh38
NC_000022.10:g.38129354C>G , CM000684.1:g.38129354C>G GRCh37
NC_000022.9:g.36459300C>G NCBI36
NG_012857.1:g.41360C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3997C>G MANE Select ENSP00000496394.1:p.Gln1333Glu
ENST00000344404.10:c.*3480C>G ENSP00000340312.6:n.*3480C>G
ENST00000406386.7:c.3997C>G ENSP00000384312.3:p.Gln1333Glu
NM_001039141.2:c.3997C>G NP_001034230.1:p.Gln1333Glu
XM_011530646.1:c.512-2988G>C XP_011528948.1:n.512-2988G>C
NM_001039141.3:c.3997C>G MANE Select NP_001034230.1:p.Gln1333Glu
Search 100 bp 5'
Search 100 bp 3'