Canonical Allele Identifier: CA392819922

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64455136A>G (hg19) ; chr15:g.64162937A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162937A>G , CM000677.2:g.64162937A>G	GRCh38
NC_000015.9:g.64455136A>G , CM000677.1:g.64455136A>G	GRCh37
NC_000015.8:g.62242189A>G	NCBI36
NG_012979.1:g.5219T>C , LRG_10:g.5219T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.50T>C MANE Select	ENSP00000300026.4:p.Leu17Pro
ENST00000561048.2:n.83T>C
ENST00000680158.1:c.50T>C	ENSP00000504873.1:p.Leu17Pro
ENST00000681397.1:c.50T>C	ENSP00000506584.1:p.Leu17Pro
ENST00000681658.1:c.30+20T>C	ENSP00000505431.1:n.30+20T>C
ENST00000300026.3:c.50T>C	ENSP00000300026.3:p.Leu17Pro
ENST00000558492.1:n.70T>C
ENST00000561048.1:n.85T>C
NM_000942.4:c.50T>C , LRG_10t1:c.50T>C	NP_000933.1:p.Leu17Pro
NM_000942.5:c.50T>C MANE Select	NP_000933.1:p.Leu17Pro