Canonical Allele Identifier: CA2404484378
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733152_37733153delinsAG , CM000684.2:g.37733152_37733153delinsAG GRCh38
NC_000022.10:g.38129159_38129160delinsAG , CM000684.1:g.38129159_38129160delinsAG GRCh37
NC_000022.9:g.36459105_36459106delinsAG NCBI36
NG_012857.1:g.41165_41166delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-146_3948-145delinsAG MANE Select ENSP00000496394.1:n.3948-146_3948-145delinsAG
ENST00000344404.10:c.*3431-146_*3431-145delinsAG ENSP00000340312.6:n.*3431-146_*3431-145delinsAG
ENST00000406386.7:c.3948-146_3948-145delinsAG ENSP00000384312.3:n.3948-146_3948-145delinsAG
NM_001039141.2:c.3948-146_3948-145delinsAG NP_001034230.1:n.3948-146_3948-145delinsAG
XM_011530646.1:c.512-2794_512-2793delinsCT XP_011528948.1:n.512-2794_512-2793delinsCT
NM_001039141.3:c.3948-146_3948-145delinsAG MANE Select NP_001034230.1:n.3948-146_3948-145delinsAG