Canonical Allele Identifier: CA392817699

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452312C>A (hg19) ; chr15:g.64160113C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160113C>A , CM000677.2:g.64160113C>A	GRCh38
NC_000015.9:g.64452312C>A , CM000677.1:g.64452312C>A	GRCh37
NC_000015.8:g.62239365C>A	NCBI36
NG_012979.1:g.8043G>T , LRG_10:g.8043G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.334G>T MANE Select	ENSP00000300026.4:p.Gly112Cys
ENST00000561048.2:n.367G>T
ENST00000680158.1:c.334G>T	ENSP00000504873.1:p.Gly112Cys
ENST00000680343.1:n.288G>T
ENST00000681397.1:c.334G>T	ENSP00000506584.1:p.Gly112Cys
ENST00000681658.1:c.229G>T	ENSP00000505431.1:p.Gly77Cys
ENST00000300026.3:c.334G>T	ENSP00000300026.3:p.Gly112Cys
ENST00000558492.1:n.240G>T
ENST00000561048.1:n.369G>T
NM_000942.4:c.334G>T , LRG_10t1:c.334G>T	NP_000933.1:p.Gly112Cys
NM_000942.5:c.334G>T MANE Select	NP_000933.1:p.Gly112Cys