Canonical Allele Identifier: CA2628934212

Gene: PPIB

Linked Data

• gnomAD v4: 15-64162781-T-TGAGCCAAGGCTGAGCCAAGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162791_64162792insTGAGCCAAGGCCGAGCCAAGGC , CM000677.2:g.64162791_64162792insTGAGCCAAGGCCGAGCCAAGGC	GRCh38
NC_000015.9:g.64454990_64454991insTGAGCCAAGGCCGAGCCAAGGC , CM000677.1:g.64454990_64454991insTGAGCCAAGGCCGAGCCAAGGC	GRCh37
NC_000015.8:g.62242043_62242044insTGAGCCAAGGCCGAGCCAAGGC	NCBI36
NG_012979.1:g.5374_5375insGGCCTTGGCTCAGCCTTGGCTC , LRG_10:g.5374_5375insGGCCTTGGCTCAGCCTTGGCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC MANE Select	ENSP00000300026.4:n.135+70_135+71insGGCCT...
ENST00000561048.2:n.168+70_168+71insGGCCTTGGCTCAGCCTTGGCTC
ENST00000680158.1:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC	ENSP00000504873.1:n.135+70_135+71insGGCCT...
ENST00000681397.1:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC	ENSP00000506584.1:n.135+70_135+71insGGCCT...
ENST00000681658.1:c.30+175_30+176insGGCCTTGGCTCAGCCTTGGCTC	ENSP00000505431.1:n.30+175_30+176insGGCCT...
ENST00000300026.3:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC	ENSP00000300026.3:n.135+70_135+71insGGCCT...
ENST00000558492.1:n.155+70_155+71insGGCCTTGGCTCAGCCTTGGCTC
ENST00000561048.1:n.170+70_170+71insGGCCTTGGCTCAGCCTTGGCTC
NM_000942.4:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC , LRG_10t1:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC	NP_000933.1:n.135+70_135+71insGGCCTTGGCTC...
NM_000942.5:c.135+70_135+71insGGCCTTGGCTCAGCCTTGGCTC MANE Select	NP_000933.1:n.135+70_135+71insGGCCTTGGCTC...