Canonical Allele Identifier: CA1770489799

Gene: PPP3CC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22540901G= , CM000670.2:g.22540901G=	GRCh38
NC_000008.10:g.22398414G= , CM000670.1:g.22398414G=	GRCh37
NC_000008.9:g.22454359G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005605.5:c.*99G= MANE Select	NP_005596.2:n.*99G=
ENST00000240139.10:c.*99G= MANE Select	ENSP00000240139.5:n.*99G=
NM_001243974.1:c.*99G=	NP_001230903.1:n.*99G=
NM_001243974.2:c.*99G=	NP_001230903.1:n.*99G=
NM_001243975.1:c.*99G=	NP_001230904.1:n.*99G=
NM_001243975.2:c.*99G=	NP_001230904.1:n.*99G=
NM_005605.4:c.*99G=	NP_005596.2:n.*99G=
ENST00000240139.9:c.*99G=	ENSP00000240139.5:n.*99G=
ENST00000289963.12:c.*99G=	ENSP00000289963.8:n.*99G=
ENST00000397775.7:c.*99G=	ENSP00000380878.3:n.*99G=
XM_005273564.1:c.*99G=	XP_005273621.1:n.*99G=
XM_011544572.1:c.*99G=	XP_011542874.1:n.*99G=
XR_001745553.2:n.2170G=
XR_001745554.2:n.2433G=
XR_001745555.2:n.2109G=
XR_001745556.2:n.2079G=
XR_001745557.2:n.2547G=
XR_001745558.2:n.2284G=