Canonical Allele Identifier: CA490814612

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64455105C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162906C>T , CM000677.2:g.64162906C>T	GRCh38
NC_000015.9:g.64455105C>T , CM000677.1:g.64455105C>T	GRCh37
NC_000015.8:g.62242158C>T	NCBI36
NG_012979.1:g.5250G>A , LRG_10:g.5250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.81G>A MANE Select	ENSP00000300026.4:p.Leu27=
ENST00000561048.2:n.114G>A
ENST00000680158.1:c.81G>A	ENSP00000504873.1:p.Leu27=
ENST00000681397.1:c.81G>A	ENSP00000506584.1:p.Leu27=
ENST00000681658.1:c.30+51G>A	ENSP00000505431.1:n.30+51G>A
ENST00000300026.3:c.81G>A	ENSP00000300026.3:p.Leu27=
ENST00000558492.1:n.101G>A
ENST00000561048.1:n.116G>A
NM_000942.4:c.81G>A , LRG_10t1:c.81G>A	NP_000933.1:p.Leu27=
NM_000942.5:c.81G>A MANE Select	NP_000933.1:p.Leu27=