Canonical Allele Identifier: CA392817732

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452315C>T (hg19) ; chr15:g.64160116C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160116C>T , CM000677.2:g.64160116C>T	GRCh38
NC_000015.9:g.64452315C>T , CM000677.1:g.64452315C>T	GRCh37
NC_000015.8:g.62239368C>T	NCBI36
NG_012979.1:g.8040G>A , LRG_10:g.8040G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.331G>A MANE Select	ENSP00000300026.4:p.Asp111Asn
ENST00000561048.2:n.364G>A
ENST00000680158.1:c.331G>A	ENSP00000504873.1:p.Asp111Asn
ENST00000680343.1:n.285G>A
ENST00000681397.1:c.331G>A	ENSP00000506584.1:p.Asp111Asn
ENST00000681658.1:c.226G>A	ENSP00000505431.1:p.Asp76Asn
ENST00000300026.3:c.331G>A	ENSP00000300026.3:p.Asp111Asn
ENST00000558492.1:n.237G>A
ENST00000561048.1:n.366G>A
NM_000942.4:c.331G>A , LRG_10t1:c.331G>A	NP_000933.1:p.Asp111Asn
NM_000942.5:c.331G>A MANE Select	NP_000933.1:p.Asp111Asn