Canonical Allele Identifier: CA10224671
Community Standard Title: NM_001039141.3(TRIOBP):c.5380-19C>G
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37754858C>G , CM000684.2:g.37754858C>G GRCh38
NC_000022.10:g.38150865C>G , CM000684.1:g.38150865C>G GRCh37
NC_000022.9:g.36480811C>G NCBI36
NG_012857.1:g.62871C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001039141.3:c.5380-19C>G MANE Select NP_001034230.1:n.5380-19C>G
ENST00000644935.1:c.5380-19C>G MANE Select ENSP00000496394.1:n.5380-19C>G
NM_001039141.2:c.5380-19C>G NP_001034230.1:n.5380-19C>G
NM_007032.5:c.241-19C>G NP_008963.3:n.241-19C>G
NM_138632.2:c.241-19C>G NP_619538.2:n.241-19C>G
ENST00000344404.10:c.*4863-19C>G ENSP00000340312.6:n.*4863-19C>G
ENST00000403663.6:c.241-19C>G ENSP00000386026.2:n.241-19C>G
ENST00000406386.7:c.5380-19C>G ENSP00000384312.3:n.5380-19C>G
ENST00000407319.6:c.241-19C>G ENSP00000383913.2:n.241-19C>G
ENST00000407319.7:c.241-19C>G ENSP00000383913.2:n.241-19C>G
ENST00000413051.2:c.246-19C>G ENSP00000400680.2:n.246-19C>G
ENST00000417857.1:c.28-19C>G ENSP00000387881.1:n.28-19C>G
ENST00000418339.5:c.118-19C>G ENSP00000396946.1:n.118-19C>G
ENST00000428075.5:c.209-243C>G
ENST00000452519.5:c.28-19C>G ENSP00000407542.1:n.28-19C>G