Canonical Allele Identifier: CA2183002593

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64156692_64156703delinsTGCCCAGTAGTA , CM000677.2:g.64156692_64156703delinsTGCCCAGTAGTA GRCh38
NC_000015.9:g.64448891_64448902delinsTGCCCAGTAGTA , CM000677.1:g.64448891_64448902delinsTGCCCAGTAGTA GRCh37
NC_000015.8:g.62235944_62235955delinsTGCCCAGTAGTA NCBI36
NG_012979.1:g.11453_11464delinsTACTACTGGGCA , LRG_10:g.11453_11464delinsTACTACTGGGCA
NG_033071.1:g.9976_9987delinsTGCCCAGTAGTA

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.528+22_528+33delinsTACTACTGGGCA (PPIB) MANE Select ENSP00000300026.4:n.528+22_528+33delinsTA...
ENST00000325881.9:c.*2184_*2195delinsTGCCCAGTAGTA (SNX22) MANE Select ENSP00000323435.4:n.*2184_*2195delinsTGCC...
ENST00000561048.2:n.3755+22_3755+33delinsTACTACTGGGCA (PPIB)
ENST00000680158.1:c.*201+22_*201+33delinsTACTACTGGGCA (PPIB) ENSP00000504873.1:n.*201+22_*201+33delins...
ENST00000680343.1:n.482+22_482+33delinsTACTACTGGGCA (PPIB)
ENST00000681397.1:c.528+22_528+33delinsTACTACTGGGCA (PPIB) ENSP00000506584.1:n.528+22_528+33delinsTA...
ENST00000681658.1:c.423+22_423+33delinsTACTACTGGGCA (PPIB) ENSP00000505431.1:n.423+22_423+33delinsTA...
ENST00000300026.3:c.528+22_528+33delinsTACTACTGGGCA (PPIB) ENSP00000300026.3:n.528+22_528+33delinsTA...
ENST00000325881.8:c.*2184_*2195delinsTGCCCAGTAGTA (SNX22) ENSP00000323435.4:n.*2184_*2195delinsTGCC...
ENST00000557789.5:n.2924_2935delinsTGCCCAGTAGTA (SNX22)
ENST00000560997.1:n.2579_2590delinsTGCCCAGTAGTA (SNX22)
NM_000942.4:c.528+22_528+33delinsTACTACTGGGCA , LRG_10t1:c.528+22_528+33delinsTACTACTGGGCA (PPIB) NP_000933.1:n.528+22_528+33delinsTACTACTG...
NM_024798.2:c.*2184_*2195delinsTGCCCAGTAGTA (SNX22) NP_079074.2:n.*2184_*2195delinsTGCCCAGTAG...
NR_073534.1:n.2872_2883delinsTGCCCAGTAGTA (SNX22)
XM_017022581.1:c.*2184_*2195delinsTGCCCAGTAGTA (SNX22) XP_016878070.1:n.*2184_*2195delinsTGCCCAG...
NM_024798.3:c.*2184_*2195delinsTGCCCAGTAGTA (SNX22) MANE Select NP_079074.2:n.*2184_*2195delinsTGCCCAGTAG...
NM_000942.5:c.528+22_528+33delinsTACTACTGGGCA (PPIB) MANE Select NP_000933.1:n.528+22_528+33delinsTACTACTG...
NR_073534.2:n.2858_2869delinsTGCCCAGTAGTA (SNX22)