Canonical Allele Identifier: CA10223350
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs749995384
ExAC: 22:38109469 TGCA / T
gnomAD v2: 22-38109469-TGCA-T
gnomAD v3: 22-37713462-TGCA-T
gnomAD v4: 22-37713462-TGCA-T
MyVariant Identifiers: chr22:g.38109470_38109472del (hg19) chr22:g.37713464_37713466del (hg38) chr22:g.37713463_37713465del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713465_37713467del , CM000684.2:g.37713465_37713467del GRCh38
NC_000022.10:g.38109472_38109474del , CM000684.1:g.38109472_38109474del GRCh37
NC_000022.9:g.36439418_36439420del NCBI36
NG_012857.1:g.21478_21480del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.456+54_456+56del MANE Select ENSP00000496394.1:n.456+54_456+56del
ENST00000344404.10:c.255-2298_255-2296del ENSP00000340312.6:n.255-2298_255-2296del
ENST00000406386.7:c.456+54_456+56del ENSP00000384312.3:n.456+54_456+56del
ENST00000455236.4:c.1413+54_1413+56del ENSP00000477208.1:n.1413+54_1413+56del
ENST00000492485.5:n.391-2298_391-2296del
NM_001039141.2:c.456+54_456+56del NP_001034230.1:n.456+54_456+56del
NM_001039141.3:c.456+54_456+56del MANE Select NP_001034230.1:n.456+54_456+56del
Search 100 bp 5'
Search 100 bp 3'