Canonical Allele Identifier: CA1111747447

Gene: PPP3CC

Linked Data

• dbSNP Id: rs1837413490
• gnomAD v3: 8-22463153-G-GA
• gnomAD v4: 8-22463153-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22463155dup , CM000670.2:g.22463155dup	GRCh38
NC_000008.10:g.22320668dup , CM000670.1:g.22320668dup	GRCh37
NC_000008.9:g.22376613dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000240139.10:c.50-11799dup MANE Select	ENSP00000240139.5:n.50-11799dup
ENST00000240139.9:c.50-11799dup	ENSP00000240139.5:n.50-11799dup
ENST00000289963.12:c.50-11799dup	ENSP00000289963.8:n.50-11799dup
ENST00000397775.7:c.50-11799dup	ENSP00000380878.3:n.50-11799dup
ENST00000518852.5:c.50-11799dup	ENSP00000429379.1:n.50-11799dup
ENST00000522000.1:c.95-11799dup	ENSP00000428358.1:n.95-11799dup
NM_001243974.1:c.50-11799dup	NP_001230903.1:n.50-11799dup
NM_001243975.1:c.50-11799dup	NP_001230904.1:n.50-11799dup
NM_005605.4:c.50-11799dup	NP_005596.2:n.50-11799dup
XM_005273564.1:c.50-11799dup	XP_005273621.1:n.50-11799dup
XR_949434.1:n.490-11799dup
XR_949436.1:n.490-11799dup
XM_017013611.2:c.50-11799dup	XP_016869100.1:n.50-11799dup
XR_001745553.2:n.407-11799dup
XR_001745554.2:n.407-11799dup
XR_001745555.2:n.407-11799dup
XR_001745556.2:n.407-11799dup
XR_001745557.2:n.407-11799dup
XR_001745558.2:n.407-11799dup
XR_001745559.2:n.407-11799dup
NM_001243974.2:c.50-11799dup	NP_001230903.1:n.50-11799dup
NM_001243975.2:c.50-11799dup	NP_001230904.1:n.50-11799dup
NM_005605.5:c.50-11799dup MANE Select	NP_005596.2:n.50-11799dup