Canonical Allele Identifier: CA2183005502
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162869G= , CM000677.2:g.64162869G= GRCh38
NC_000015.9:g.64455068G= , CM000677.1:g.64455068G= GRCh37
NC_000015.8:g.62242121G= NCBI36
NG_012979.1:g.5287C= , LRG_10:g.5287C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.118C= MANE Select ENSP00000300026.4:p.Pro40=
ENST00000561048.2:n.151C=
ENST00000680158.1:c.118C= ENSP00000504873.1:p.Pro40=
ENST00000681397.1:c.118C= ENSP00000506584.1:p.Pro40=
ENST00000681658.1:c.30+88C= ENSP00000505431.1:n.30+88C=
ENST00000300026.3:c.118C= ENSP00000300026.3:p.Pro40=
ENST00000558492.1:n.138C=
ENST00000561048.1:n.153C=
NM_000942.4:c.118C= , LRG_10t1:c.118C= NP_000933.1:p.Pro40=
NM_000942.5:c.118C= MANE Select NP_000933.1:p.Pro40=