Canonical Allele Identifier: CA411487072
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38129314G>T (hg19) chr22:g.37733307G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733307G>T , CM000684.2:g.37733307G>T GRCh38
NC_000022.10:g.38129314G>T , CM000684.1:g.38129314G>T GRCh37
NC_000022.9:g.36459260G>T NCBI36
NG_012857.1:g.41320G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3957G>T MANE Select ENSP00000496394.1:p.Glu1319Asp
ENST00000344404.10:c.*3440G>T ENSP00000340312.6:n.*3440G>T
ENST00000406386.7:c.3957G>T ENSP00000384312.3:p.Glu1319Asp
NM_001039141.2:c.3957G>T NP_001034230.1:p.Glu1319Asp
XM_011530646.1:c.512-2948C>A XP_011528948.1:n.512-2948C>A
NM_001039141.3:c.3957G>T MANE Select NP_001034230.1:p.Glu1319Asp
Search 100 bp 5'
Search 100 bp 3'