Canonical Allele Identifier: CA490812800

Gene: PPIB

Linked Data

• MyVariant Identifiers: chr15:g.64452310G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64160111G>C , CM000677.2:g.64160111G>C	GRCh38
NC_000015.9:g.64452310G>C , CM000677.1:g.64452310G>C	GRCh37
NC_000015.8:g.62239363G>C	NCBI36
NG_012979.1:g.8045C>G , LRG_10:g.8045C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.336C>G MANE Select	ENSP00000300026.4:p.Gly112=
ENST00000561048.2:n.369C>G
ENST00000680158.1:c.336C>G	ENSP00000504873.1:p.Gly112=
ENST00000680343.1:n.290C>G
ENST00000681397.1:c.336C>G	ENSP00000506584.1:p.Gly112=
ENST00000681658.1:c.231C>G	ENSP00000505431.1:p.Gly77=
ENST00000300026.3:c.336C>G	ENSP00000300026.3:p.Gly112=
ENST00000558492.1:n.242C>G
ENST00000561048.1:n.371C>G
NM_000942.4:c.336C>G , LRG_10t1:c.336C>G	NP_000933.1:p.Gly112=
NM_000942.5:c.336C>G MANE Select	NP_000933.1:p.Gly112=