Canonical Allele Identifier: CA102979844

Gene: PPP3CA

Linked Data

• dbSNP Id: rs373856643
• MyVariant Identifiers: chr4:g.102047976G>T (hg19) ; chr4:g.101126819G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101126819G>T , CM000666.2:g.101126819G>T	GRCh38
NC_000004.11:g.102047976G>T , CM000666.1:g.102047976G>T	GRCh37
NC_000004.10:g.102266999G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394854.8:c.260-17741C>A MANE Select	ENSP00000378323.3:n.260-17741C>A
ENST00000323055.10:c.260-17741C>A	ENSP00000320580.6:n.260-17741C>A
ENST00000394853.8:c.260-17741C>A	ENSP00000378322.4:n.260-17741C>A
ENST00000394854.7:c.260-17741C>A	ENSP00000378323.3:n.260-17741C>A
ENST00000492351.6:c.157-17741C>A	ENSP00000426565.1:n.157-17741C>A
ENST00000507176.5:c.-35-17741C>A	ENSP00000422990.1:n.-35-17741C>A
ENST00000510292.1:n.151-17741C>A
ENST00000512215.5:c.260-63462C>A	ENSP00000422781.1:n.260-63462C>A
ENST00000525819.1:c.110-17741C>A	ENSP00000434599.1:n.110-17741C>A
ENST00000529324.5:c.110-17741C>A	ENSP00000431619.1:n.110-17741C>A
NM_000944.4:c.260-17741C>A	NP_000935.1:n.260-17741C>A
NM_001130691.1:c.260-17741C>A	NP_001124163.1:n.260-17741C>A
NM_001130692.1:c.260-17741C>A	NP_001124164.1:n.260-17741C>A
XM_017008365.1:c.224-17741C>A	XP_016863854.1:n.224-17741C>A
XM_024454127.1:c.110-17741C>A	XP_024309895.1:n.110-17741C>A
NM_000944.5:c.260-17741C>A MANE Select	NP_000935.1:n.260-17741C>A
NM_001130691.2:c.260-17741C>A	NP_001124163.1:n.260-17741C>A
NM_001130692.2:c.260-17741C>A	NP_001124164.1:n.260-17741C>A