Canonical Allele Identifier: CA2183005450
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162782_64162793delinsGAGCCAAGGCCA , CM000677.2:g.64162782_64162793delinsGAGCCAAGGCCA GRCh38
NC_000015.9:g.64454981_64454992delinsGAGCCAAGGCCA , CM000677.1:g.64454981_64454992delinsGAGCCAAGGCCA GRCh37
NC_000015.8:g.62242034_62242045delinsGAGCCAAGGCCA NCBI36
NG_012979.1:g.5363_5374delinsTGGCCTTGGCTC , LRG_10:g.5363_5374delinsTGGCCTTGGCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+59_135+70delinsTGGCCTTGGCTC MANE Select ENSP00000300026.4:n.135+59_135+70delinsTG...
ENST00000561048.2:n.168+59_168+70delinsTGGCCTTGGCTC
ENST00000680158.1:c.135+59_135+70delinsTGGCCTTGGCTC ENSP00000504873.1:n.135+59_135+70delinsTG...
ENST00000681397.1:c.135+59_135+70delinsTGGCCTTGGCTC ENSP00000506584.1:n.135+59_135+70delinsTG...
ENST00000681658.1:c.30+164_30+175delinsTGGCCTTGGCTC ENSP00000505431.1:n.30+164_30+175delinsTG...
ENST00000300026.3:c.135+59_135+70delinsTGGCCTTGGCTC ENSP00000300026.3:n.135+59_135+70delinsTG...
ENST00000558492.1:n.155+59_155+70delinsTGGCCTTGGCTC
ENST00000561048.1:n.170+59_170+70delinsTGGCCTTGGCTC
NM_000942.4:c.135+59_135+70delinsTGGCCTTGGCTC , LRG_10t1:c.135+59_135+70delinsTGGCCTTGGCTC NP_000933.1:n.135+59_135+70delinsTGGCCTTG...
NM_000942.5:c.135+59_135+70delinsTGGCCTTGGCTC MANE Select NP_000933.1:n.135+59_135+70delinsTGGCCTTG...