Canonical Allele Identifier: CA2183004187
Gene: PPIB HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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