Canonical Allele Identifier: CA7608556

Gene: PPIB

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162022C>A , CM000677.2:g.64162022C>A	GRCh38
NC_000015.9:g.64454221C>A , CM000677.1:g.64454221C>A	GRCh37
NC_000015.8:g.62241274C>A	NCBI36
NG_012979.1:g.6134G>T , LRG_10:g.6134G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.249+19G>T MANE Select	ENSP00000300026.4:n.249+19G>T
ENST00000561048.2:n.282+19G>T
ENST00000680158.1:c.249+19G>T	ENSP00000504873.1:n.249+19G>T
ENST00000680343.1:n.203+19G>T
ENST00000681397.1:c.253+15G>T	ENSP00000506584.1:n.253+15G>T
ENST00000681658.1:c.144+19G>T	ENSP00000505431.1:n.144+19G>T
ENST00000300026.3:c.249+19G>T	ENSP00000300026.3:n.249+19G>T
ENST00000558492.1:n.155+830G>T
ENST00000561048.1:n.284+19G>T
NM_000942.4:c.249+19G>T , LRG_10t1:c.249+19G>T	NP_000933.1:n.249+19G>T
NM_000942.5:c.249+19G>T MANE Select	NP_000933.1:n.249+19G>T