Canonical Allele Identifier: CA1770430093

Gene: PPP3CC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22463223T= , CM000670.2:g.22463223T=	GRCh38
NC_000008.10:g.22320736T= , CM000670.1:g.22320736T=	GRCh37
NC_000008.9:g.22376681T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000240139.10:c.50-11731T= MANE Select	ENSP00000240139.5:n.50-11731T=
ENST00000240139.9:c.50-11731T=	ENSP00000240139.5:n.50-11731T=
ENST00000289963.12:c.50-11731T=	ENSP00000289963.8:n.50-11731T=
ENST00000397775.7:c.50-11731T=	ENSP00000380878.3:n.50-11731T=
ENST00000518852.5:c.50-11731T=	ENSP00000429379.1:n.50-11731T=
ENST00000522000.1:c.95-11731T=	ENSP00000428358.1:n.95-11731T=
NM_001243974.1:c.50-11731T=	NP_001230903.1:n.50-11731T=
NM_001243975.1:c.50-11731T=	NP_001230904.1:n.50-11731T=
NM_005605.4:c.50-11731T=	NP_005596.2:n.50-11731T=
XM_005273564.1:c.50-11731T=	XP_005273621.1:n.50-11731T=
XR_949434.1:n.490-11731T=
XR_949436.1:n.490-11731T=
XM_017013611.2:c.50-11731T=	XP_016869100.1:n.50-11731T=
XR_001745553.2:n.407-11731T=
XR_001745554.2:n.407-11731T=
XR_001745555.2:n.407-11731T=
XR_001745556.2:n.407-11731T=
XR_001745557.2:n.407-11731T=
XR_001745558.2:n.407-11731T=
XR_001745559.2:n.407-11731T=
NM_001243974.2:c.50-11731T=	NP_001230903.1:n.50-11731T=
NM_001243975.2:c.50-11731T=	NP_001230904.1:n.50-11731T=
NM_005605.5:c.50-11731T= MANE Select	NP_005596.2:n.50-11731T=