Canonical Allele Identifier: CA2183005444
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162779G= , CM000677.2:g.64162779G= GRCh38
NC_000015.9:g.64454978G= , CM000677.1:g.64454978G= GRCh37
NC_000015.8:g.62242031G= NCBI36
NG_012979.1:g.5377C= , LRG_10:g.5377C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+73C= MANE Select ENSP00000300026.4:n.135+73C=
ENST00000561048.2:n.168+73C=
ENST00000680158.1:c.135+73C= ENSP00000504873.1:n.135+73C=
ENST00000681397.1:c.135+73C= ENSP00000506584.1:n.135+73C=
ENST00000681658.1:c.30+178C= ENSP00000505431.1:n.30+178C=
ENST00000300026.3:c.135+73C= ENSP00000300026.3:n.135+73C=
ENST00000558492.1:n.155+73C=
ENST00000561048.1:n.170+73C=
NM_000942.4:c.135+73C= , LRG_10t1:c.135+73C= NP_000933.1:n.135+73C=
NM_000942.5:c.135+73C= MANE Select NP_000933.1:n.135+73C=