Canonical Allele Identifier: CA2183004185
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160108T= , CM000677.2:g.64160108T= GRCh38
NC_000015.9:g.64452307T= , CM000677.1:g.64452307T= GRCh37
NC_000015.8:g.62239360T= NCBI36
NG_012979.1:g.8048A= , LRG_10:g.8048A=

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.339A= MANE Select ENSP00000300026.4:p.Thr113=
ENST00000561048.2:n.372A=
ENST00000680158.1:c.339A= ENSP00000504873.1:p.Thr113=
ENST00000680343.1:n.293A=
ENST00000681397.1:c.339A= ENSP00000506584.1:p.Thr113=
ENST00000681658.1:c.234A= ENSP00000505431.1:p.Thr78=
ENST00000300026.3:c.339A= ENSP00000300026.3:p.Thr113=
ENST00000558492.1:n.245A=
ENST00000561048.1:n.374A=
NM_000942.4:c.339A= , LRG_10t1:c.339A= NP_000933.1:p.Thr113=
NM_000942.5:c.339A= MANE Select NP_000933.1:p.Thr113=