Canonical Allele Identifier: CA2404484383
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1924505367

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733159_37733164del , CM000684.2:g.37733159_37733164del GRCh38
NC_000022.10:g.38129166_38129171del , CM000684.1:g.38129166_38129171del GRCh37
NC_000022.9:g.36459112_36459117del NCBI36
NG_012857.1:g.41172_41177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-139_3948-134del MANE Select ENSP00000496394.1:n.3948-139_3948-134del
ENST00000344404.10:c.*3431-139_*3431-134del ENSP00000340312.6:n.*3431-139_*3431-134del
ENST00000406386.7:c.3948-139_3948-134del ENSP00000384312.3:n.3948-139_3948-134del
NM_001039141.2:c.3948-139_3948-134del NP_001034230.1:n.3948-139_3948-134del
XM_011530646.1:c.512-2802_512-2797del XP_011528948.1:n.512-2802_512-2797del
NM_001039141.3:c.3948-139_3948-134del MANE Select NP_001034230.1:n.3948-139_3948-134del