Canonical Allele Identifier: CA10225044
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37765831_37765832insC , CM000684.2:g.37765831_37765832insC GRCh38
NC_000022.10:g.38161838_38161839insC , CM000684.1:g.38161838_38161839insC GRCh37
NC_000022.9:g.36491784_36491785insC NCBI36
NG_012857.1:g.73844_73845insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6472+14_6472+15insC MANE Select ENSP00000496394.1:n.6472+14_6472+15insC
ENST00000344404.10:c.*5955+14_*5955+15insC ENSP00000340312.6:n.*5955+14_*5955+15insC
ENST00000403663.6:c.1333+14_1333+15insC ENSP00000386026.2:n.1333+14_1333+15insC
ENST00000406386.7:c.6472+14_6472+15insC ENSP00000384312.3:n.6472+14_6472+15insC
NM_001039141.2:c.6472+14_6472+15insC NP_001034230.1:n.6472+14_6472+15insC
NM_007032.5:c.1333+14_1333+15insC NP_008963.3:n.1333+14_1333+15insC
NM_001039141.3:c.6472+14_6472+15insC MANE Select NP_001034230.1:n.6472+14_6472+15insC