Canonical Allele Identifier: CA392817662

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452303C>A (hg19) ; chr15:g.64160104C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160104C>A , CM000677.2:g.64160104C>A	GRCh38
NC_000015.9:g.64452303C>A , CM000677.1:g.64452303C>A	GRCh37
NC_000015.8:g.62239356C>A	NCBI36
NG_012979.1:g.8052G>T , LRG_10:g.8052G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.343G>T MANE Select	ENSP00000300026.4:p.Gly115Ter
ENST00000561048.2:n.376G>T
ENST00000680158.1:c.343G>T	ENSP00000504873.1:p.Gly115Ter
ENST00000680343.1:n.297G>T
ENST00000681397.1:c.343G>T	ENSP00000506584.1:p.Gly115Ter
ENST00000681658.1:c.238G>T	ENSP00000505431.1:p.Gly80Ter
ENST00000300026.3:c.343G>T	ENSP00000300026.3:p.Gly115Ter
ENST00000558492.1:n.249G>T
ENST00000561048.1:n.378G>T
NM_000942.4:c.343G>T , LRG_10t1:c.343G>T	NP_000933.1:p.Gly115Ter
NM_000942.5:c.343G>T MANE Select	NP_000933.1:p.Gly115Ter