Canonical Allele Identifier: CA1770407045

Gene: PPP3CC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22447518_22447521delinsCTGT , CM000670.2:g.22447518_22447521delinsCTGT	GRCh38
NC_000008.10:g.22305031_22305034delinsCTGT , CM000670.1:g.22305031_22305034delinsCTGT	GRCh37
NC_000008.9:g.22360976_22360979delinsCTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000240139.10:c.49+6060_49+6063delinsCTGT MANE Select	ENSP00000240139.5:n.49+6060_49+6063delins...
ENST00000240139.9:c.49+6060_49+6063delinsCTGT	ENSP00000240139.5:n.49+6060_49+6063delins...
ENST00000289963.12:c.49+6060_49+6063delinsCTGT	ENSP00000289963.8:n.49+6060_49+6063delins...
ENST00000397775.7:c.49+6060_49+6063delinsCTGT	ENSP00000380878.3:n.49+6060_49+6063delins...
ENST00000518852.5:c.49+6060_49+6063delinsCTGT	ENSP00000429379.1:n.49+6060_49+6063delins...
ENST00000522000.1:c.94+6060_94+6063delinsCTGT	ENSP00000428358.1:n.94+6060_94+6063delins...
NM_001243974.1:c.49+6060_49+6063delinsCTGT	NP_001230903.1:n.49+6060_49+6063delinsCTG...
NM_001243975.1:c.49+6060_49+6063delinsCTGT	NP_001230904.1:n.49+6060_49+6063delinsCTG...
NM_005605.4:c.49+6060_49+6063delinsCTGT	NP_005596.2:n.49+6060_49+6063delinsCTGT
XM_005273564.1:c.49+6060_49+6063delinsCTGT	XP_005273621.1:n.49+6060_49+6063delinsCTG...
XR_949434.1:n.489+6060_489+6063delinsCTGT
XR_949436.1:n.489+6060_489+6063delinsCTGT
XM_017013611.2:c.49+6060_49+6063delinsCTGT	XP_016869100.1:n.49+6060_49+6063delinsCTG...
XR_001745553.2:n.406+6060_406+6063delinsCTGT
XR_001745554.2:n.406+6060_406+6063delinsCTGT
XR_001745555.2:n.406+6060_406+6063delinsCTGT
XR_001745556.2:n.406+6060_406+6063delinsCTGT
XR_001745557.2:n.406+6060_406+6063delinsCTGT
XR_001745558.2:n.406+6060_406+6063delinsCTGT
XR_001745559.2:n.406+6060_406+6063delinsCTGT
NM_001243974.2:c.49+6060_49+6063delinsCTGT	NP_001230903.1:n.49+6060_49+6063delinsCTG...
NM_001243975.2:c.49+6060_49+6063delinsCTGT	NP_001230904.1:n.49+6060_49+6063delinsCTG...
NM_005605.5:c.49+6060_49+6063delinsCTGT MANE Select	NP_005596.2:n.49+6060_49+6063delinsCTGT