Canonical Allele Identifier: CA324121304
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs902222580
gnomAD v2: 22-38111931-G-GA
gnomAD v4: 22-37715924-G-GA
MyVariant Identifiers: chr22:g.38111931_38111932insA (hg19) chr22:g.37715924_37715925insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715929dup , CM000684.2:g.37715929dup GRCh38
NC_000022.10:g.38111936dup , CM000684.1:g.38111936dup GRCh37
NC_000022.9:g.36441882dup NCBI36
NG_012857.1:g.23942dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.623dup MANE Select ENSP00000496394.1:p.Glu209GlyfsTer?
ENST00000344404.10:c.*106dup ENSP00000340312.6:n.*106dup
ENST00000406386.7:c.623dup ENSP00000384312.3:p.Glu209GlyfsTer?
ENST00000455236.4:c.1580dup ENSP00000477208.1:n.1580dup
ENST00000492485.5:n.557dup
NM_001039141.2:c.623dup NP_001034230.1:p.Glu209GlyfsTer?
NM_001039141.3:c.623dup MANE Select NP_001034230.1:p.Glu209GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'