Canonical Allele Identifier: CA392817676

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452308G>C (hg19) ; chr15:g.64160109G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160109G>C , CM000677.2:g.64160109G>C	GRCh38
NC_000015.9:g.64452308G>C , CM000677.1:g.64452308G>C	GRCh37
NC_000015.8:g.62239361G>C	NCBI36
NG_012979.1:g.8047C>G , LRG_10:g.8047C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.338C>G MANE Select	ENSP00000300026.4:p.Thr113Arg
ENST00000561048.2:n.371C>G
ENST00000680158.1:c.338C>G	ENSP00000504873.1:p.Thr113Arg
ENST00000680343.1:n.292C>G
ENST00000681397.1:c.338C>G	ENSP00000506584.1:p.Thr113Arg
ENST00000681658.1:c.233C>G	ENSP00000505431.1:p.Thr78Arg
ENST00000300026.3:c.338C>G	ENSP00000300026.3:p.Thr113Arg
ENST00000558492.1:n.244C>G
ENST00000561048.1:n.373C>G
NM_000942.4:c.338C>G , LRG_10t1:c.338C>G	NP_000933.1:p.Thr113Arg
NM_000942.5:c.338C>G MANE Select	NP_000933.1:p.Thr113Arg