Canonical Allele Identifier: CA2183005549
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162961A= , CM000677.2:g.64162961A= GRCh38
NC_000015.9:g.64455160A= , CM000677.1:g.64455160A= GRCh37
NC_000015.8:g.62242213A= NCBI36
NG_012979.1:g.5195T= , LRG_10:g.5195T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.26T= MANE Select ENSP00000300026.4:p.Met9=
ENST00000561048.2:n.59T=
ENST00000680158.1:c.26T= ENSP00000504873.1:p.Met9=
ENST00000681397.1:c.26T= ENSP00000506584.1:p.Met9=
ENST00000681658.1:c.26T= ENSP00000505431.1:p.Met9=
ENST00000300026.3:c.26T= ENSP00000300026.3:p.Met9=
ENST00000558492.1:n.46T=
ENST00000561048.1:n.61T=
NM_000942.4:c.26T= , LRG_10t1:c.26T= NP_000933.1:p.Met9=
NM_000942.5:c.26T= MANE Select NP_000933.1:p.Met9=