Canonical Allele Identifier: CA2404495373
Community Standard Title: NM_001039141.3(TRIOBP):c.5488-2A=
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37755099A= , CM000684.2:g.37755099A= GRCh38
NC_000022.10:g.38151106A= , CM000684.1:g.38151106A= GRCh37
NC_000022.9:g.36481052A= NCBI36
NG_012857.1:g.63112A=

Transcript Alleles

HGVS Amino-acid Change
NM_001039141.3:c.5488-2A= MANE Select NP_001034230.1:n.5488-2A=
ENST00000644935.1:c.5488-2A= MANE Select ENSP00000496394.1:n.5488-2A=
NM_001039141.2:c.5488-2A= NP_001034230.1:n.5488-2A=
NM_007032.5:c.349-2A= NP_008963.3:n.349-2A=
NM_138632.2:c.349-2A= NP_619538.2:n.349-2A=
ENST00000331103.5:n.104-2A=
ENST00000344404.10:c.*4971-2A= ENSP00000340312.6:n.*4971-2A=
ENST00000403663.6:c.349-2A= ENSP00000386026.2:n.349-2A=
ENST00000406386.7:c.5488-2A= ENSP00000384312.3:n.5488-2A=
ENST00000407319.6:c.349-2A= ENSP00000383913.2:n.349-2A=
ENST00000407319.7:c.349-2A= ENSP00000383913.2:n.349-2A=
ENST00000413051.2:c.354-2A= ENSP00000400680.2:n.354-2A=
ENST00000417857.1:c.136-2A= ENSP00000387881.1:n.136-2A=
ENST00000418339.5:c.226-2A= ENSP00000396946.1:n.226-2A=
ENST00000428075.5:c.209-2A=
ENST00000452519.5:c.136-2A= ENSP00000407542.1:n.136-2A=