Canonical Allele Identifier: CA639194034
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1303991252
gnomAD v2: 22-38106646-T-TC
gnomAD v3: 22-37710639-T-TC
gnomAD v4: 22-37710639-T-TC
MyVariant Identifiers: chr22:g.38106646_38106647insC (hg19) chr22:g.37710639_37710640insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710643dup , CM000684.2:g.37710643dup GRCh38
NC_000022.10:g.38106650dup , CM000684.1:g.38106650dup GRCh37
NC_000022.9:g.36436596dup NCBI36
NG_012857.1:g.18656dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.254+77dup MANE Select ENSP00000496394.1:n.254+77dup
ENST00000344404.10:c.254+77dup ENSP00000340312.6:n.254+77dup
ENST00000406386.7:c.254+77dup ENSP00000384312.3:n.254+77dup
ENST00000455236.4:c.1211+77dup ENSP00000477208.1:n.1211+77dup
ENST00000492485.5:n.390+77dup
NM_001039141.2:c.254+77dup NP_001034230.1:n.254+77dup
NM_001039141.3:c.254+77dup MANE Select NP_001034230.1:n.254+77dup
Search 100 bp 5'
Search 100 bp 3'