Canonical Allele Identifier: CA411510298
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768127A>T , CM000684.2:g.37768127A>T GRCh38
NC_000022.10:g.38164134A>T , CM000684.1:g.38164134A>T GRCh37
NC_000022.9:g.36494080A>T NCBI36
NG_012857.1:g.76140A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6526A>T MANE Select ENSP00000496394.1:p.Lys2176Ter
ENST00000344404.10:c.*6009A>T ENSP00000340312.6:n.*6009A>T
ENST00000403663.6:c.1387A>T ENSP00000386026.2:p.Lys463Ter
ENST00000406386.7:c.6526A>T ENSP00000384312.3:p.Lys2176Ter
NM_001039141.2:c.6526A>T NP_001034230.1:p.Lys2176Ter
NM_007032.5:c.1387A>T NP_008963.3:p.Lys463Ter
NM_001039141.3:c.6526A>T MANE Select NP_001034230.1:p.Lys2176Ter