Canonical Allele Identifier: CA392817664

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452305C>A (hg19) ; chr15:g.64160106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160106C>A , CM000677.2:g.64160106C>A	GRCh38
NC_000015.9:g.64452305C>A , CM000677.1:g.64452305C>A	GRCh37
NC_000015.8:g.62239358C>A	NCBI36
NG_012979.1:g.8050G>T , LRG_10:g.8050G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.341G>T MANE Select	ENSP00000300026.4:p.Gly114Val
ENST00000561048.2:n.374G>T
ENST00000680158.1:c.341G>T	ENSP00000504873.1:p.Gly114Val
ENST00000680343.1:n.295G>T
ENST00000681397.1:c.341G>T	ENSP00000506584.1:p.Gly114Val
ENST00000681658.1:c.236G>T	ENSP00000505431.1:p.Gly79Val
ENST00000300026.3:c.341G>T	ENSP00000300026.3:p.Gly114Val
ENST00000558492.1:n.247G>T
ENST00000561048.1:n.376G>T
NM_000942.4:c.341G>T , LRG_10t1:c.341G>T	NP_000933.1:p.Gly114Val
NM_000942.5:c.341G>T MANE Select	NP_000933.1:p.Gly114Val