Canonical Allele Identifier: CA2183005511

Gene: PPIB

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162891C= , CM000677.2:g.64162891C=	GRCh38
NC_000015.9:g.64455090C= , CM000677.1:g.64455090C=	GRCh37
NC_000015.8:g.62242143C=	NCBI36
NG_012979.1:g.5265G= , LRG_10:g.5265G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.96G= MANE Select	ENSP00000300026.4:p.Ala32=
ENST00000561048.2:n.129G=
ENST00000680158.1:c.96G=	ENSP00000504873.1:p.Ala32=
ENST00000681397.1:c.96G=	ENSP00000506584.1:p.Ala32=
ENST00000681658.1:c.30+66G=	ENSP00000505431.1:n.30+66G=
ENST00000300026.3:c.96G=	ENSP00000300026.3:p.Ala32=
ENST00000558492.1:n.116G=
ENST00000561048.1:n.131G=
NM_000942.4:c.96G= , LRG_10t1:c.96G=	NP_000933.1:p.Ala32=
NM_000942.5:c.96G= MANE Select	NP_000933.1:p.Ala32=