Canonical Allele Identifier: CA324140996
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs950948012

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733168_37733170del , CM000684.2:g.37733168_37733170del GRCh38
NC_000022.10:g.38129175_38129177del , CM000684.1:g.38129175_38129177del GRCh37
NC_000022.9:g.36459121_36459123del NCBI36
NG_012857.1:g.41181_41183del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-130_3948-128del MANE Select ENSP00000496394.1:n.3948-130_3948-128del
ENST00000344404.10:c.*3431-130_*3431-128del ENSP00000340312.6:n.*3431-130_*3431-128del
ENST00000406386.7:c.3948-130_3948-128del ENSP00000384312.3:n.3948-130_3948-128del
NM_001039141.2:c.3948-130_3948-128del NP_001034230.1:n.3948-130_3948-128del
XM_011530646.1:c.512-2811_512-2809del XP_011528948.1:n.512-2811_512-2809del
NM_001039141.3:c.3948-130_3948-128del MANE Select NP_001034230.1:n.3948-130_3948-128del