Canonical Allele Identifier: CA392819831
Gene: PPIB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162889G>C , CM000677.2:g.64162889G>C GRCh38
NC_000015.9:g.64455088G>C , CM000677.1:g.64455088G>C GRCh37
NC_000015.8:g.62242141G>C NCBI36
NG_012979.1:g.5267C>G , LRG_10:g.5267C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300026.4:c.98C>G MANE Select ENSP00000300026.4:p.Ala33Gly
ENST00000561048.2:n.131C>G
ENST00000680158.1:c.98C>G ENSP00000504873.1:p.Ala33Gly
ENST00000681397.1:c.98C>G ENSP00000506584.1:p.Ala33Gly
ENST00000681658.1:c.30+68C>G ENSP00000505431.1:n.30+68C>G
ENST00000300026.3:c.98C>G ENSP00000300026.3:p.Ala33Gly
ENST00000558492.1:n.118C>G
ENST00000561048.1:n.133C>G
NM_000942.4:c.98C>G , LRG_10t1:c.98C>G NP_000933.1:p.Ala33Gly
NM_000942.5:c.98C>G MANE Select NP_000933.1:p.Ala33Gly