Canonical Allele Identifier: CA411447079
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710538G>T , CM000684.2:g.37710538G>T GRCh38
NC_000022.10:g.38106545G>T , CM000684.1:g.38106545G>T GRCh37
NC_000022.9:g.36436491G>T NCBI36
NG_012857.1:g.18551G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.226G>T MANE Select ENSP00000496394.1:p.Asp76Tyr
ENST00000344404.10:c.226G>T ENSP00000340312.6:p.Asp76Tyr
ENST00000406386.7:c.226G>T ENSP00000384312.3:p.Asp76Tyr
ENST00000455236.4:c.1183G>T ENSP00000477208.1:n.1183G>T
ENST00000492485.5:n.362G>T
NM_001039141.2:c.226G>T NP_001034230.1:p.Asp76Tyr
NM_001039141.3:c.226G>T MANE Select NP_001034230.1:p.Asp76Tyr