Canonical Allele Identifier: CA411487393
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38129379A>T (hg19) chr22:g.37733372A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733372A>T , CM000684.2:g.37733372A>T GRCh38
NC_000022.10:g.38129379A>T , CM000684.1:g.38129379A>T GRCh37
NC_000022.9:g.36459325A>T NCBI36
NG_012857.1:g.41385A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4022A>T MANE Select ENSP00000496394.1:p.Gln1341Leu
ENST00000344404.10:c.*3505A>T ENSP00000340312.6:n.*3505A>T
ENST00000406386.7:c.4022A>T ENSP00000384312.3:p.Gln1341Leu
NM_001039141.2:c.4022A>T NP_001034230.1:p.Gln1341Leu
XM_011530646.1:c.512-3013T>A XP_011528948.1:n.512-3013T>A
NM_001039141.3:c.4022A>T MANE Select NP_001034230.1:p.Gln1341Leu
Search 100 bp 5'
Search 100 bp 3'