Canonical Allele Identifier: CA656187497

Gene: PPIB

Linked Data

• COSMIC: COSN24941893

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162782_64162783insGAGCCAAGGCC , CM000677.2:g.64162782_64162783insGAGCCAAGGCC	GRCh38
NC_000015.9:g.64454981_64454982insGAGCCAAGGCC , CM000677.1:g.64454981_64454982insGAGCCAAGGCC	GRCh37
NC_000015.8:g.62242034_62242035insGAGCCAAGGCC	NCBI36
NG_012979.1:g.5373_5374insGGCCTTGGCTC , LRG_10:g.5373_5374insGGCCTTGGCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+69_135+70insGGCCTTGGCTC MANE Select	ENSP00000300026.4:n.135+69_135+70insGGCCT...
ENST00000561048.2:n.168+69_168+70insGGCCTTGGCTC
ENST00000680158.1:c.135+69_135+70insGGCCTTGGCTC	ENSP00000504873.1:n.135+69_135+70insGGCCT...
ENST00000681397.1:c.135+69_135+70insGGCCTTGGCTC	ENSP00000506584.1:n.135+69_135+70insGGCCT...
ENST00000681658.1:c.30+174_30+175insGGCCTTGGCTC	ENSP00000505431.1:n.30+174_30+175insGGCCT...
ENST00000300026.3:c.135+69_135+70insGGCCTTGGCTC	ENSP00000300026.3:n.135+69_135+70insGGCCT...
ENST00000558492.1:n.155+69_155+70insGGCCTTGGCTC
ENST00000561048.1:n.170+69_170+70insGGCCTTGGCTC
NM_000942.4:c.135+69_135+70insGGCCTTGGCTC , LRG_10t1:c.135+69_135+70insGGCCTTGGCTC	NP_000933.1:n.135+69_135+70insGGCCTTGGCTC...
NM_000942.5:c.135+69_135+70insGGCCTTGGCTC MANE Select	NP_000933.1:n.135+69_135+70insGGCCTTGGCTC...