Canonical Allele Identifier: CA392817712

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452313A>T (hg19) ; chr15:g.64160114A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160114A>T , CM000677.2:g.64160114A>T	GRCh38
NC_000015.9:g.64452313A>T , CM000677.1:g.64452313A>T	GRCh37
NC_000015.8:g.62239366A>T	NCBI36
NG_012979.1:g.8042T>A , LRG_10:g.8042T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.333T>A MANE Select	ENSP00000300026.4:p.Asp111Glu
ENST00000561048.2:n.366T>A
ENST00000680158.1:c.333T>A	ENSP00000504873.1:p.Asp111Glu
ENST00000680343.1:n.287T>A
ENST00000681397.1:c.333T>A	ENSP00000506584.1:p.Asp111Glu
ENST00000681658.1:c.228T>A	ENSP00000505431.1:p.Asp76Glu
ENST00000300026.3:c.333T>A	ENSP00000300026.3:p.Asp111Glu
ENST00000558492.1:n.239T>A
ENST00000561048.1:n.368T>A
NM_000942.4:c.333T>A , LRG_10t1:c.333T>A	NP_000933.1:p.Asp111Glu
NM_000942.5:c.333T>A MANE Select	NP_000933.1:p.Asp111Glu