Canonical Allele Identifier: CA392817670
Gene: PPIB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160107C>A , CM000677.2:g.64160107C>A GRCh38
NC_000015.9:g.64452306C>A , CM000677.1:g.64452306C>A GRCh37
NC_000015.8:g.62239359C>A NCBI36
NG_012979.1:g.8049G>T , LRG_10:g.8049G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.340G>T MANE Select ENSP00000300026.4:p.Gly114Ter
ENST00000561048.2:n.373G>T
ENST00000680158.1:c.340G>T ENSP00000504873.1:p.Gly114Ter
ENST00000680343.1:n.294G>T
ENST00000681397.1:c.340G>T ENSP00000506584.1:p.Gly114Ter
ENST00000681658.1:c.235G>T ENSP00000505431.1:p.Gly79Ter
ENST00000300026.3:c.340G>T ENSP00000300026.3:p.Gly114Ter
ENST00000558492.1:n.246G>T
ENST00000561048.1:n.375G>T
NM_000942.4:c.340G>T , LRG_10t1:c.340G>T NP_000933.1:p.Gly114Ter
NM_000942.5:c.340G>T MANE Select NP_000933.1:p.Gly114Ter