Canonical Allele Identifier: CA490814646

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64455111C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162912C>A , CM000677.2:g.64162912C>A	GRCh38
NC_000015.9:g.64455111C>A , CM000677.1:g.64455111C>A	GRCh37
NC_000015.8:g.62242164C>A	NCBI36
NG_012979.1:g.5244G>T , LRG_10:g.5244G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.75G>T MANE Select	ENSP00000300026.4:p.Leu25=
ENST00000561048.2:n.108G>T
ENST00000680158.1:c.75G>T	ENSP00000504873.1:p.Leu25=
ENST00000681397.1:c.75G>T	ENSP00000506584.1:p.Leu25=
ENST00000681658.1:c.30+45G>T	ENSP00000505431.1:n.30+45G>T
ENST00000300026.3:c.75G>T	ENSP00000300026.3:p.Leu25=
ENST00000558492.1:n.95G>T
ENST00000561048.1:n.110G>T
NM_000942.4:c.75G>T , LRG_10t1:c.75G>T	NP_000933.1:p.Leu25=
NM_000942.5:c.75G>T MANE Select	NP_000933.1:p.Leu25=