Canonical Allele Identifier: CA392817691

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452311C>T (hg19) ; chr15:g.64160112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160112C>T , CM000677.2:g.64160112C>T	GRCh38
NC_000015.9:g.64452311C>T , CM000677.1:g.64452311C>T	GRCh37
NC_000015.8:g.62239364C>T	NCBI36
NG_012979.1:g.8044G>A , LRG_10:g.8044G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.335G>A MANE Select	ENSP00000300026.4:p.Gly112Asp
ENST00000561048.2:n.368G>A
ENST00000680158.1:c.335G>A	ENSP00000504873.1:p.Gly112Asp
ENST00000680343.1:n.289G>A
ENST00000681397.1:c.335G>A	ENSP00000506584.1:p.Gly112Asp
ENST00000681658.1:c.230G>A	ENSP00000505431.1:p.Gly77Asp
ENST00000300026.3:c.335G>A	ENSP00000300026.3:p.Gly112Asp
ENST00000558492.1:n.241G>A
ENST00000561048.1:n.370G>A
NM_000942.4:c.335G>A , LRG_10t1:c.335G>A	NP_000933.1:p.Gly112Asp
NM_000942.5:c.335G>A MANE Select	NP_000933.1:p.Gly112Asp