Canonical Allele Identifier: CA639194048
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1427101904
gnomAD v2: 22-38106741-G-GA
gnomAD v3: 22-37710734-G-GA
gnomAD v4: 22-37710734-G-GA
MyVariant Identifiers: chr22:g.38106741_38106742insA (hg19) chr22:g.37710734_37710735insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710734_37710735insA , CM000684.2:g.37710734_37710735insA GRCh38
NC_000022.10:g.38106741_38106742insA , CM000684.1:g.38106741_38106742insA GRCh37
NC_000022.9:g.36436687_36436688insA NCBI36
NG_012857.1:g.18747_18748insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.254+168_254+169insA MANE Select ENSP00000496394.1:n.254+168_254+169insA
ENST00000344404.10:c.254+168_254+169insA ENSP00000340312.6:n.254+168_254+169insA
ENST00000406386.7:c.254+168_254+169insA ENSP00000384312.3:n.254+168_254+169insA
ENST00000455236.4:c.1211+168_1211+169insA ENSP00000477208.1:n.1211+168_1211+169insA
ENST00000492485.5:n.390+168_390+169insA
NM_001039141.2:c.254+168_254+169insA NP_001034230.1:n.254+168_254+169insA
NM_001039141.3:c.254+168_254+169insA MANE Select NP_001034230.1:n.254+168_254+169insA
Search 100 bp 5'
Search 100 bp 3'