Canonical Allele Identifier: CA490812791

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452304T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160105T>A , CM000677.2:g.64160105T>A	GRCh38
NC_000015.9:g.64452304T>A , CM000677.1:g.64452304T>A	GRCh37
NC_000015.8:g.62239357T>A	NCBI36
NG_012979.1:g.8051A>T , LRG_10:g.8051A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.342A>T MANE Select	ENSP00000300026.4:p.Gly114=
ENST00000561048.2:n.375A>T
ENST00000680158.1:c.342A>T	ENSP00000504873.1:p.Gly114=
ENST00000680343.1:n.296A>T
ENST00000681397.1:c.342A>T	ENSP00000506584.1:p.Gly114=
ENST00000681658.1:c.237A>T	ENSP00000505431.1:p.Gly79=
ENST00000300026.3:c.342A>T	ENSP00000300026.3:p.Gly114=
ENST00000558492.1:n.248A>T
ENST00000561048.1:n.377A>T
NM_000942.4:c.342A>T , LRG_10t1:c.342A>T	NP_000933.1:p.Gly114=
NM_000942.5:c.342A>T MANE Select	NP_000933.1:p.Gly114=