Canonical Allele Identifier: CA2183005510
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162884C= , CM000677.2:g.64162884C= GRCh38
NC_000015.9:g.64455083C= , CM000677.1:g.64455083C= GRCh37
NC_000015.8:g.62242136C= NCBI36
NG_012979.1:g.5272G= , LRG_10:g.5272G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.103G= MANE Select ENSP00000300026.4:p.Glu35=
ENST00000561048.2:n.136G=
ENST00000680158.1:c.103G= ENSP00000504873.1:p.Glu35=
ENST00000681397.1:c.103G= ENSP00000506584.1:p.Glu35=
ENST00000681658.1:c.30+73G= ENSP00000505431.1:n.30+73G=
ENST00000300026.3:c.103G= ENSP00000300026.3:p.Glu35=
ENST00000558492.1:n.123G=
ENST00000561048.1:n.138G=
NM_000942.4:c.103G= , LRG_10t1:c.103G= NP_000933.1:p.Glu35=
NM_000942.5:c.103G= MANE Select NP_000933.1:p.Glu35=