Canonical Allele Identifier: CA2404473233
Gene: TRIOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37710662_37710674delinsAATGGCTGCTGGC , CM000684.2:g.37710662_37710674delinsAATGGCTGCTGGC GRCh38
NC_000022.10:g.38106669_38106681delinsAATGGCTGCTGGC , CM000684.1:g.38106669_38106681delinsAATGGCTGCTGGC GRCh37
NC_000022.9:g.36436615_36436627delinsAATGGCTGCTGGC NCBI36
NG_012857.1:g.18675_18687delinsAATGGCTGCTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.254+96_254+108delinsAATGGCTGCTGGC MANE Select ENSP00000496394.1:n.254+96_254+108delinsAATGGCTGCTGGC
ENST00000344404.10:c.254+96_254+108delinsAATGGCTGCTGGC ENSP00000340312.6:n.254+96_254+108delinsAATGGCTGCTGGC
ENST00000406386.7:c.254+96_254+108delinsAATGGCTGCTGGC ENSP00000384312.3:n.254+96_254+108delinsAATGGCTGCTGGC
ENST00000455236.4:c.1211+96_1211+108delinsAATGGCTGCTGGC ENSP00000477208.1:n.1211+96_1211+108delinsAATGGCTGCTGGC
ENST00000492485.5:n.390+96_390+108delinsAATGGCTGCTGGC
NM_001039141.2:c.254+96_254+108delinsAATGGCTGCTGGC NP_001034230.1:n.254+96_254+108delinsAATGGCTGCTGGC
NM_001039141.3:c.254+96_254+108delinsAATGGCTGCTGGC MANE Select NP_001034230.1:n.254+96_254+108delinsAATGGCTGCTGGC