Canonical Allele Identifier: CA411487474
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733389T>G , CM000684.2:g.37733389T>G GRCh38
NC_000022.10:g.38129396T>G , CM000684.1:g.38129396T>G GRCh37
NC_000022.9:g.36459342T>G NCBI36
NG_012857.1:g.41402T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4039T>G MANE Select ENSP00000496394.1:p.Ser1347Ala
ENST00000344404.10:c.*3522T>G ENSP00000340312.6:n.*3522T>G
ENST00000406386.7:c.4039T>G ENSP00000384312.3:p.Ser1347Ala
NM_001039141.2:c.4039T>G NP_001034230.1:p.Ser1347Ala
XM_011530646.1:c.512-3030A>C XP_011528948.1:n.512-3030A>C
NM_001039141.3:c.4039T>G MANE Select NP_001034230.1:p.Ser1347Ala