Canonical Allele Identifier: CA271414783
Community Standard Title: NM_000942.5(PPIB):c.249+163A>G
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64161878T>C , CM000677.2:g.64161878T>C GRCh38
NC_000015.9:g.64454077T>C , CM000677.1:g.64454077T>C GRCh37
NC_000015.8:g.62241130T>C NCBI36
NG_012979.1:g.6278A>G , LRG_10:g.6278A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000942.5:c.249+163A>G MANE Select NP_000933.1:n.249+163A>G
ENST00000300026.4:c.249+163A>G MANE Select ENSP00000300026.4:n.249+163A>G
NM_000942.4:c.249+163A>G , LRG_10t1:c.249+163A>G NP_000933.1:n.249+163A>G
ENST00000300026.3:c.249+163A>G ENSP00000300026.3:n.249+163A>G
ENST00000558492.1:n.155+974A>G
ENST00000561048.1:n.284+163A>G
ENST00000561048.2:n.282+163A>G
ENST00000680158.1:c.249+163A>G ENSP00000504873.1:n.249+163A>G
ENST00000680343.1:n.203+163A>G
ENST00000681397.1:c.253+159A>G ENSP00000506584.1:n.253+159A>G
ENST00000681658.1:c.144+163A>G ENSP00000505431.1:n.144+163A>G