Canonical Allele Identifier: CA1770430060
Gene: PPP3CC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22463204C= , CM000670.2:g.22463204C= GRCh38
NC_000008.10:g.22320717C= , CM000670.1:g.22320717C= GRCh37
NC_000008.9:g.22376662C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000240139.10:c.50-11750C= MANE Select ENSP00000240139.5:n.50-11750C=
ENST00000240139.9:c.50-11750C= ENSP00000240139.5:n.50-11750C=
ENST00000289963.12:c.50-11750C= ENSP00000289963.8:n.50-11750C=
ENST00000397775.7:c.50-11750C= ENSP00000380878.3:n.50-11750C=
ENST00000518852.5:c.50-11750C= ENSP00000429379.1:n.50-11750C=
ENST00000522000.1:c.95-11750C= ENSP00000428358.1:n.95-11750C=
NM_001243974.1:c.50-11750C= NP_001230903.1:n.50-11750C=
NM_001243975.1:c.50-11750C= NP_001230904.1:n.50-11750C=
NM_005605.4:c.50-11750C= NP_005596.2:n.50-11750C=
XM_005273564.1:c.50-11750C= XP_005273621.1:n.50-11750C=
XR_949434.1:n.490-11750C=
XR_949436.1:n.490-11750C=
XM_017013611.2:c.50-11750C= XP_016869100.1:n.50-11750C=
XR_001745553.2:n.407-11750C=
XR_001745554.2:n.407-11750C=
XR_001745555.2:n.407-11750C=
XR_001745556.2:n.407-11750C=
XR_001745557.2:n.407-11750C=
XR_001745558.2:n.407-11750C=
XR_001745559.2:n.407-11750C=
NM_001243974.2:c.50-11750C= NP_001230903.1:n.50-11750C=
NM_001243975.2:c.50-11750C= NP_001230904.1:n.50-11750C=
NM_005605.5:c.50-11750C= MANE Select NP_005596.2:n.50-11750C=