Canonical Allele Identifier: CA2843661135
Gene: TRIOBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715969T>A , CM000684.2:g.37715969T>A GRCh38
NC_000022.10:g.38111976T>A , CM000684.1:g.38111976T>A GRCh37
NC_000022.9:g.36441922T>A NCBI36
NG_012857.1:g.23982T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.628+35T>A MANE Select ENSP00000496394.1:n.628+35T>A
ENST00000344404.10:c.*111+35T>A ENSP00000340312.6:n.*111+35T>A
ENST00000406386.7:c.628+35T>A ENSP00000384312.3:n.628+35T>A
ENST00000455236.4:c.1585+35T>A ENSP00000477208.1:n.1585+35T>A
ENST00000492485.5:n.562+35T>A
NM_001039141.2:c.628+35T>A NP_001034230.1:n.628+35T>A
NM_001039141.3:c.628+35T>A MANE Select NP_001034230.1:n.628+35T>A
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