Canonical Allele Identifier: CA10223319
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs772663057

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713302A>G , CM000684.2:g.37713302A>G GRCh38
NC_000022.10:g.38109309A>G , CM000684.1:g.38109309A>G GRCh37
NC_000022.9:g.36439255A>G NCBI36
NG_012857.1:g.21315A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.347A>G MANE Select ENSP00000496394.1:p.Glu116Gly
ENST00000344404.10:c.255-2461A>G ENSP00000340312.6:n.255-2461A>G
ENST00000406386.7:c.347A>G ENSP00000384312.3:p.Glu116Gly
ENST00000455236.4:c.1304A>G ENSP00000477208.1:n.1304A>G
ENST00000492485.5:n.391-2461A>G
NM_001039141.2:c.347A>G NP_001034230.1:p.Glu116Gly
NM_001039141.3:c.347A>G MANE Select NP_001034230.1:p.Glu116Gly