Canonical Allele Identifier: CA411487326
Gene: TRIOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733361A>C , CM000684.2:g.37733361A>C GRCh38
NC_000022.10:g.38129368A>C , CM000684.1:g.38129368A>C GRCh37
NC_000022.9:g.36459314A>C NCBI36
NG_012857.1:g.41374A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4011A>C MANE Select ENSP00000496394.1:p.Gln1337His
ENST00000344404.10:c.*3494A>C ENSP00000340312.6:n.*3494A>C
ENST00000406386.7:c.4011A>C ENSP00000384312.3:p.Gln1337His
NM_001039141.2:c.4011A>C NP_001034230.1:p.Gln1337His
XM_011530646.1:c.512-3002T>G XP_011528948.1:n.512-3002T>G
NM_001039141.3:c.4011A>C MANE Select NP_001034230.1:p.Gln1337His