Canonical Allele Identifier: CA1770484723

Gene: PPP3CC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22528966C= , CM000670.2:g.22528966C=	GRCh38
NC_000008.10:g.22386479C= , CM000670.1:g.22386479C=	GRCh37
NC_000008.9:g.22442424C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240139.10:c.1141+389C= MANE Select	ENSP00000240139.5:n.1141+389C=
ENST00000240139.9:c.1141+389C=	ENSP00000240139.5:n.1141+389C=
ENST00000289963.12:c.1141+389C=	ENSP00000289963.8:n.1141+389C=
ENST00000397775.7:c.1141+389C=	ENSP00000380878.3:n.1141+389C=
NM_001243974.1:c.1141+389C=	NP_001230903.1:n.1141+389C=
NM_001243975.1:c.1141+389C=	NP_001230904.1:n.1141+389C=
NM_005605.4:c.1141+389C=	NP_005596.2:n.1141+389C=
XM_005273564.1:c.1141+389C=	XP_005273621.1:n.1141+389C=
XM_011544572.1:c.619+389C=	XP_011542874.1:n.619+389C=
XR_949434.1:n.1581+389C=
XM_017013611.2:c.1141+389C=	XP_016869100.1:n.1141+389C=
XR_001745553.2:n.1498+389C=
XR_001745554.2:n.1498+389C=
XR_001745555.2:n.1612+389C=
XR_001745556.2:n.1612+389C=
XR_001745557.2:n.1612+389C=
XR_001745558.2:n.1612+389C=
NM_001243974.2:c.1141+389C=	NP_001230903.1:n.1141+389C=
NM_001243975.2:c.1141+389C=	NP_001230904.1:n.1141+389C=
NM_005605.5:c.1141+389C= MANE Select	NP_005596.2:n.1141+389C=