Canonical Allele Identifier: CA392819933

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64455142G>C (hg19) ; chr15:g.64162943G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162943G>C , CM000677.2:g.64162943G>C	GRCh38
NC_000015.9:g.64455142G>C , CM000677.1:g.64455142G>C	GRCh37
NC_000015.8:g.62242195G>C	NCBI36
NG_012979.1:g.5213C>G , LRG_10:g.5213C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.44C>G MANE Select	ENSP00000300026.4:p.Ala15Gly
ENST00000561048.2:n.77C>G
ENST00000680158.1:c.44C>G	ENSP00000504873.1:p.Ala15Gly
ENST00000681397.1:c.44C>G	ENSP00000506584.1:p.Ala15Gly
ENST00000681658.1:c.30+14C>G	ENSP00000505431.1:n.30+14C>G
ENST00000300026.3:c.44C>G	ENSP00000300026.3:p.Ala15Gly
ENST00000558492.1:n.64C>G
ENST00000561048.1:n.79C>G
NM_000942.4:c.44C>G , LRG_10t1:c.44C>G	NP_000933.1:p.Ala15Gly
NM_000942.5:c.44C>G MANE Select	NP_000933.1:p.Ala15Gly