Canonical Allele Identifier: CA2183004183
Gene: PPIB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64160103C= , CM000677.2:g.64160103C= GRCh38
NC_000015.9:g.64452302C= , CM000677.1:g.64452302C= GRCh37
NC_000015.8:g.62239355C= NCBI36
NG_012979.1:g.8053G= , LRG_10:g.8053G=

Transcript Alleles

HGVS Amino-acid change
ENST00000300026.4:c.343+1G= MANE Select ENSP00000300026.4:n.343+1G=
ENST00000561048.2:n.377G=
ENST00000680158.1:c.343+1G= ENSP00000504873.1:n.343+1G=
ENST00000680343.1:n.297+1G=
ENST00000681397.1:c.343+1G= ENSP00000506584.1:n.343+1G=
ENST00000681658.1:c.238+1G= ENSP00000505431.1:n.238+1G=
ENST00000300026.3:c.343+1G= ENSP00000300026.3:n.343+1G=
ENST00000558492.1:n.249+1G=
ENST00000561048.1:n.379G=
NM_000942.4:c.343+1G= , LRG_10t1:c.343+1G= NP_000933.1:n.343+1G=
NM_000942.5:c.343+1G= MANE Select NP_000933.1:n.343+1G=