Canonical Allele Identifier: CA271414554
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64161703C>A , CM000677.2:g.64161703C>A GRCh38
NC_000015.9:g.64453902C>A , CM000677.1:g.64453902C>A GRCh37
NC_000015.8:g.62240955C>A NCBI36
NG_012979.1:g.6453G>T , LRG_10:g.6453G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.249+338G>T MANE Select ENSP00000300026.4:n.249+338G>T
ENST00000561048.2:n.282+338G>T
ENST00000680158.1:c.249+338G>T ENSP00000504873.1:n.249+338G>T
ENST00000680343.1:n.203+338G>T
ENST00000681397.1:c.253+334G>T ENSP00000506584.1:n.253+334G>T
ENST00000681658.1:c.144+338G>T ENSP00000505431.1:n.144+338G>T
ENST00000300026.3:c.249+338G>T ENSP00000300026.3:n.249+338G>T
ENST00000558492.1:n.155+1149G>T
ENST00000561048.1:n.284+338G>T
NM_000942.4:c.249+338G>T , LRG_10t1:c.249+338G>T NP_000933.1:n.249+338G>T
NM_000942.5:c.249+338G>T MANE Select NP_000933.1:n.249+338G>T