Canonical Allele Identifier: CA7608557
Community Standard Title: NM_000942.5(PPIB):c.249+12G>A
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64162029C>T , CM000677.2:g.64162029C>T GRCh38
NC_000015.9:g.64454228C>T , CM000677.1:g.64454228C>T GRCh37
NC_000015.8:g.62241281C>T NCBI36
NG_012979.1:g.6127G>A , LRG_10:g.6127G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000942.5:c.249+12G>A MANE Select NP_000933.1:n.249+12G>A
ENST00000300026.4:c.249+12G>A MANE Select ENSP00000300026.4:n.249+12G>A
NM_000942.4:c.249+12G>A , LRG_10t1:c.249+12G>A NP_000933.1:n.249+12G>A
ENST00000300026.3:c.249+12G>A ENSP00000300026.3:n.249+12G>A
ENST00000558492.1:n.155+823G>A
ENST00000561048.1:n.284+12G>A
ENST00000561048.2:n.282+12G>A
ENST00000680158.1:c.249+12G>A ENSP00000504873.1:n.249+12G>A
ENST00000680343.1:n.203+12G>A
ENST00000681397.1:c.253+8G>A ENSP00000506584.1:n.253+8G>A
ENST00000681658.1:c.144+12G>A ENSP00000505431.1:n.144+12G>A