Canonical Allele Identifier: CA970720433
Gene: PPIB HGNC NCBI

Linked Data

dbSNP Id: rs2081557047

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160109_64160120dup , CM000677.2:g.64160109_64160120dup GRCh38
NC_000015.9:g.64452308_64452319dup , CM000677.1:g.64452308_64452319dup GRCh37
NC_000015.8:g.62239361_62239372dup NCBI36
NG_012979.1:g.8036_8047dup , LRG_10:g.8036_8047dup

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.327_338dup MANE Select ENSP00000300026.4:p.Thr113_Gly114insGlyAs...
ENST00000561048.2:n.360_371dup
ENST00000680158.1:c.327_338dup ENSP00000504873.1:p.Thr113_Gly114insGlyAs...
ENST00000680343.1:n.281_292dup
ENST00000681397.1:c.327_338dup ENSP00000506584.1:p.Thr113_Gly114insGlyAs...
ENST00000681658.1:c.222_233dup ENSP00000505431.1:p.Thr78_Gly79insGlyAspG...
ENST00000300026.3:c.327_338dup ENSP00000300026.3:p.Thr113_Gly114insGlyAs...
ENST00000558492.1:n.233_244dup
ENST00000561048.1:n.362_373dup
NM_000942.4:c.327_338dup , LRG_10t1:c.327_338dup NP_000933.1:p.Thr113_Gly114insGlyAspGlyTh...
NM_000942.5:c.327_338dup MANE Select NP_000933.1:p.Thr113_Gly114insGlyAspGlyTh...