Canonical Allele Identifier: CA514771491
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38119919A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37723912A>T , CM000684.2:g.37723912A>T GRCh38
NC_000022.10:g.38119919A>T , CM000684.1:g.38119919A>T GRCh37
NC_000022.9:g.36449865A>T NCBI36
NG_012857.1:g.31925A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.1356A>T MANE Select ENSP00000496394.1:p.Thr452=
ENST00000344404.10:c.*839A>T ENSP00000340312.6:n.*839A>T
ENST00000406386.7:c.1356A>T ENSP00000384312.3:p.Thr452=
ENST00000455236.4:c.2313A>T ENSP00000477208.1:n.2313A>T
ENST00000492485.5:n.1290A>T
NM_001039141.2:c.1356A>T NP_001034230.1:p.Thr452=
NM_001039141.3:c.1356A>T MANE Select NP_001034230.1:p.Thr452=
Search 100 bp 5'
Search 100 bp 3'