Canonical Allele Identifier: CA2404484392
Gene: TRIOBP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733192G= , CM000684.2:g.37733192G= GRCh38
NC_000022.10:g.38129199G= , CM000684.1:g.38129199G= GRCh37
NC_000022.9:g.36459145G= NCBI36
NG_012857.1:g.41205G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-106G= MANE Select ENSP00000496394.1:n.3948-106G=
ENST00000344404.10:c.*3431-106G= ENSP00000340312.6:n.*3431-106G=
ENST00000406386.7:c.3948-106G= ENSP00000384312.3:n.3948-106G=
NM_001039141.2:c.3948-106G= NP_001034230.1:n.3948-106G=
XM_011530646.1:c.512-2833C= XP_011528948.1:n.512-2833C=
NM_001039141.3:c.3948-106G= MANE Select NP_001034230.1:n.3948-106G=
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