Canonical Allele Identifier: CA392819858

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64455103G>A (hg19) ; chr15:g.64162904G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162904G>A , CM000677.2:g.64162904G>A	GRCh38
NC_000015.9:g.64455103G>A , CM000677.1:g.64455103G>A	GRCh37
NC_000015.8:g.62242156G>A	NCBI36
NG_012979.1:g.5252C>T , LRG_10:g.5252C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.83C>T MANE Select	ENSP00000300026.4:p.Pro28Leu
ENST00000561048.2:n.116C>T
ENST00000680158.1:c.83C>T	ENSP00000504873.1:p.Pro28Leu
ENST00000681397.1:c.83C>T	ENSP00000506584.1:p.Pro28Leu
ENST00000681658.1:c.30+53C>T	ENSP00000505431.1:n.30+53C>T
ENST00000300026.3:c.83C>T	ENSP00000300026.3:p.Pro28Leu
ENST00000558492.1:n.103C>T
ENST00000561048.1:n.118C>T
NM_000942.4:c.83C>T , LRG_10t1:c.83C>T	NP_000933.1:p.Pro28Leu
NM_000942.5:c.83C>T MANE Select	NP_000933.1:p.Pro28Leu