Canonical Allele Identifier: CA411487486
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733390C>T , CM000684.2:g.37733390C>T GRCh38
NC_000022.10:g.38129397C>T , CM000684.1:g.38129397C>T GRCh37
NC_000022.9:g.36459343C>T NCBI36
NG_012857.1:g.41403C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4040C>T MANE Select ENSP00000496394.1:p.Ser1347Phe
ENST00000344404.10:c.*3523C>T ENSP00000340312.6:n.*3523C>T
ENST00000406386.7:c.4040C>T ENSP00000384312.3:p.Ser1347Phe
NM_001039141.2:c.4040C>T NP_001034230.1:p.Ser1347Phe
XM_011530646.1:c.512-3031G>A XP_011528948.1:n.512-3031G>A
NM_001039141.3:c.4040C>T MANE Select NP_001034230.1:p.Ser1347Phe