Canonical Allele Identifier: CA392817722

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452314T>G (hg19) ; chr15:g.64160115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160115T>G , CM000677.2:g.64160115T>G	GRCh38
NC_000015.9:g.64452314T>G , CM000677.1:g.64452314T>G	GRCh37
NC_000015.8:g.62239367T>G	NCBI36
NG_012979.1:g.8041A>C , LRG_10:g.8041A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.332A>C MANE Select	ENSP00000300026.4:p.Asp111Ala
ENST00000561048.2:n.365A>C
ENST00000680158.1:c.332A>C	ENSP00000504873.1:p.Asp111Ala
ENST00000680343.1:n.286A>C
ENST00000681397.1:c.332A>C	ENSP00000506584.1:p.Asp111Ala
ENST00000681658.1:c.227A>C	ENSP00000505431.1:p.Asp76Ala
ENST00000300026.3:c.332A>C	ENSP00000300026.3:p.Asp111Ala
ENST00000558492.1:n.238A>C
ENST00000561048.1:n.367A>C
NM_000942.4:c.332A>C , LRG_10t1:c.332A>C	NP_000933.1:p.Asp111Ala
NM_000942.5:c.332A>C MANE Select	NP_000933.1:p.Asp111Ala