Canonical Allele Identifier: CA392819928
Gene: PPIB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162940G>T , CM000677.2:g.64162940G>T GRCh38
NC_000015.9:g.64455139G>T , CM000677.1:g.64455139G>T GRCh37
NC_000015.8:g.62242192G>T NCBI36
NG_012979.1:g.5216C>A , LRG_10:g.5216C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.47C>A MANE Select ENSP00000300026.4:p.Ala16Asp
ENST00000561048.2:n.80C>A
ENST00000680158.1:c.47C>A ENSP00000504873.1:p.Ala16Asp
ENST00000681397.1:c.47C>A ENSP00000506584.1:p.Ala16Asp
ENST00000681658.1:c.30+17C>A ENSP00000505431.1:n.30+17C>A
ENST00000300026.3:c.47C>A ENSP00000300026.3:p.Ala16Asp
ENST00000558492.1:n.67C>A
ENST00000561048.1:n.82C>A
NM_000942.4:c.47C>A , LRG_10t1:c.47C>A NP_000933.1:p.Ala16Asp
NM_000942.5:c.47C>A MANE Select NP_000933.1:p.Ala16Asp