Canonical Allele Identifier: CA2183005452
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162788A= , CM000677.2:g.64162788A= GRCh38
NC_000015.9:g.64454987A= , CM000677.1:g.64454987A= GRCh37
NC_000015.8:g.62242040A= NCBI36
NG_012979.1:g.5368T= , LRG_10:g.5368T=

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+64T= MANE Select ENSP00000300026.4:n.135+64T=
ENST00000561048.2:n.168+64T=
ENST00000680158.1:c.135+64T= ENSP00000504873.1:n.135+64T=
ENST00000681397.1:c.135+64T= ENSP00000506584.1:n.135+64T=
ENST00000681658.1:c.30+169T= ENSP00000505431.1:n.30+169T=
ENST00000300026.3:c.135+64T= ENSP00000300026.3:n.135+64T=
ENST00000558492.1:n.155+64T=
ENST00000561048.1:n.170+64T=
NM_000942.4:c.135+64T= , LRG_10t1:c.135+64T= NP_000933.1:n.135+64T=
NM_000942.5:c.135+64T= MANE Select NP_000933.1:n.135+64T=