Canonical Allele Identifier: CA10224561
Community Standard Title: NM_001039141.3(TRIOBP):c.5285C>T (p.Pro1762Leu)
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37740995C>T , CM000684.2:g.37740995C>T GRCh38
NC_000022.10:g.38137002C>T , CM000684.1:g.38137002C>T GRCh37
NC_000022.9:g.36466948C>T NCBI36
NG_012857.1:g.49008C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001039141.3:c.5285C>T MANE Select NP_001034230.1:p.Pro1762Leu
ENST00000644935.1:c.5285C>T MANE Select ENSP00000496394.1:p.Pro1762Leu
NM_001039141.2:c.5285C>T NP_001034230.1:p.Pro1762Leu
ENST00000344404.10:c.*4768C>T ENSP00000340312.6:n.*4768C>T
ENST00000406386.7:c.5285C>T ENSP00000384312.3:p.Pro1762Leu
XM_011530646.1:c.367-236G>A XP_011528948.1:n.367-236G>A
XM_011530647.1:c.367-236G>A XP_011528949.1:n.367-236G>A
XM_011530647.2:c.367-236G>A XP_011528949.1:n.367-236G>A
XM_017029173.1:c.19-236G>A XP_016884662.1:n.19-236G>A
XR_938241.1:n.361-236G>A
XR_938241.2:n.340-236G>A
XR_938242.1:n.314-236G>A