Canonical Allele Identifier: CA411510116
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37768089-A-G
MyVariant Identifiers: chr22:g.38164096A>G (hg19) chr22:g.37768089A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768089A>G , CM000684.2:g.37768089A>G GRCh38
NC_000022.10:g.38164096A>G , CM000684.1:g.38164096A>G GRCh37
NC_000022.9:g.36494042A>G NCBI36
NG_012857.1:g.76102A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6488A>G MANE Select ENSP00000496394.1:p.Lys2163Arg
ENST00000344404.10:c.*5971A>G ENSP00000340312.6:n.*5971A>G
ENST00000403663.6:c.1349A>G ENSP00000386026.2:p.Lys450Arg
ENST00000406386.7:c.6488A>G ENSP00000384312.3:p.Lys2163Arg
NM_001039141.2:c.6488A>G NP_001034230.1:p.Lys2163Arg
NM_007032.5:c.1349A>G NP_008963.3:p.Lys450Arg
NM_001039141.3:c.6488A>G MANE Select NP_001034230.1:p.Lys2163Arg
Search 100 bp 5'
Search 100 bp 3'