Canonical Allele Identifier: CA392819830

Gene: PPIB

Linked Data

• COSMIC: COSM6395878
• MyVariant Identifiers: chr15:g.64455088G>T (hg19) ; chr15:g.64162889G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162889G>T , CM000677.2:g.64162889G>T	GRCh38
NC_000015.9:g.64455088G>T , CM000677.1:g.64455088G>T	GRCh37
NC_000015.8:g.62242141G>T	NCBI36
NG_012979.1:g.5267C>A , LRG_10:g.5267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.98C>A MANE Select	ENSP00000300026.4:p.Ala33Asp
ENST00000561048.2:n.131C>A
ENST00000680158.1:c.98C>A	ENSP00000504873.1:p.Ala33Asp
ENST00000681397.1:c.98C>A	ENSP00000506584.1:p.Ala33Asp
ENST00000681658.1:c.30+68C>A	ENSP00000505431.1:n.30+68C>A
ENST00000300026.3:c.98C>A	ENSP00000300026.3:p.Ala33Asp
ENST00000558492.1:n.118C>A
ENST00000561048.1:n.133C>A
NM_000942.4:c.98C>A , LRG_10t1:c.98C>A	NP_000933.1:p.Ala33Asp
NM_000942.5:c.98C>A MANE Select	NP_000933.1:p.Ala33Asp