Canonical Allele Identifier: CA2575755607
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160045del , CM000677.2:g.64160045del GRCh38
NC_000015.9:g.64452244del , CM000677.1:g.64452244del GRCh37
NC_000015.8:g.62239297del NCBI36
NG_012979.1:g.8112del , LRG_10:g.8112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.343+60del MANE Select ENSP00000300026.4:n.343+60del
ENST00000561048.2:n.436del
ENST00000680158.1:c.343+60del ENSP00000504873.1:n.343+60del
ENST00000680343.1:n.297+60del
ENST00000681397.1:c.343+60del ENSP00000506584.1:n.343+60del
ENST00000681658.1:c.238+60del ENSP00000505431.1:n.238+60del
ENST00000300026.3:c.343+60del ENSP00000300026.3:n.343+60del
ENST00000558492.1:n.249+60del
ENST00000561048.1:n.438del
NM_000942.4:c.343+60del , LRG_10t1:c.343+60del NP_000933.1:n.343+60del
NM_000942.5:c.343+60del MANE Select NP_000933.1:n.343+60del