Canonical Allele Identifier: CA2628922294
Gene: PPIB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162881_64162883dup , CM000677.2:g.64162881_64162883dup GRCh38
NC_000015.9:g.64455080_64455082dup , CM000677.1:g.64455080_64455082dup GRCh37
NC_000015.8:g.62242133_62242135dup NCBI36
NG_012979.1:g.5281_5283dup , LRG_10:g.5281_5283dup

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.112_114dup MANE Select ENSP00000300026.4:p.Lys38_Gly39insLys
ENST00000561048.2:n.145_147dup
ENST00000680158.1:c.112_114dup ENSP00000504873.1:p.Lys38_Gly39insLys
ENST00000681397.1:c.112_114dup ENSP00000506584.1:p.Lys38_Gly39insLys
ENST00000681658.1:c.30+82_30+84dup ENSP00000505431.1:n.30+82_30+84dup
ENST00000300026.3:c.112_114dup ENSP00000300026.3:p.Lys38_Gly39insLys
ENST00000558492.1:n.132_134dup
ENST00000561048.1:n.147_149dup
NM_000942.4:c.112_114dup , LRG_10t1:c.112_114dup NP_000933.1:p.Lys38_Gly39insLys
NM_000942.5:c.112_114dup MANE Select NP_000933.1:p.Lys38_Gly39insLys