Canonical Allele Identifier: CA2183005439
Gene: PPIB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162770G= , CM000677.2:g.64162770G= GRCh38
NC_000015.9:g.64454969G= , CM000677.1:g.64454969G= GRCh37
NC_000015.8:g.62242022G= NCBI36
NG_012979.1:g.5386C= , LRG_10:g.5386C=

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.135+82C= MANE Select ENSP00000300026.4:n.135+82C=
ENST00000561048.2:n.168+82C=
ENST00000680158.1:c.135+82C= ENSP00000504873.1:n.135+82C=
ENST00000681397.1:c.135+82C= ENSP00000506584.1:n.135+82C=
ENST00000681658.1:c.30+187C= ENSP00000505431.1:n.30+187C=
ENST00000300026.3:c.135+82C= ENSP00000300026.3:n.135+82C=
ENST00000558492.1:n.155+82C=
ENST00000561048.1:n.170+82C=
NM_000942.4:c.135+82C= , LRG_10t1:c.135+82C= NP_000933.1:n.135+82C=
NM_000942.5:c.135+82C= MANE Select NP_000933.1:n.135+82C=
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