Canonical Allele Identifier: CA639394771
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1401583785
gnomAD v2: 22-38109160-TG-T
gnomAD v4: 22-37713153-TG-T
MyVariant Identifiers: chr22:g.38109161del (hg19) chr22:g.37713154del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713157del , CM000684.2:g.37713157del GRCh38
NC_000022.10:g.38109164del , CM000684.1:g.38109164del GRCh37
NC_000022.9:g.36439110del NCBI36
NG_012857.1:g.21170del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.255-53del MANE Select ENSP00000496394.1:n.255-53del
ENST00000344404.10:c.254+2591del ENSP00000340312.6:n.254+2591del
ENST00000406386.7:c.255-53del ENSP00000384312.3:n.255-53del
ENST00000455236.4:c.1212-53del ENSP00000477208.1:n.1212-53del
ENST00000492485.5:n.390+2591del
NM_001039141.2:c.255-53del NP_001034230.1:n.255-53del
NM_001039141.3:c.255-53del MANE Select NP_001034230.1:n.255-53del
Search 100 bp 5'
Search 100 bp 3'