Canonical Allele Identifier: CA102979848

Gene: PPP3CA

Linked Data

• dbSNP Id: rs1057349709
• gnomAD v3: 4-101126887-C-A
• gnomAD v4: 4-101126887-C-A
• MyVariant Identifiers: chr4:g.102048044C>A (hg19) ; chr4:g.101126887C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101126887C>A , CM000666.2:g.101126887C>A	GRCh38
NC_000004.11:g.102048044C>A , CM000666.1:g.102048044C>A	GRCh37
NC_000004.10:g.102267067C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394854.8:c.260-17809G>T MANE Select	ENSP00000378323.3:n.260-17809G>T
ENST00000323055.10:c.260-17809G>T	ENSP00000320580.6:n.260-17809G>T
ENST00000394853.8:c.260-17809G>T	ENSP00000378322.4:n.260-17809G>T
ENST00000394854.7:c.260-17809G>T	ENSP00000378323.3:n.260-17809G>T
ENST00000492351.6:c.157-17809G>T	ENSP00000426565.1:n.157-17809G>T
ENST00000507176.5:c.-35-17809G>T	ENSP00000422990.1:n.-35-17809G>T
ENST00000510292.1:n.151-17809G>T
ENST00000512215.5:c.260-63530G>T	ENSP00000422781.1:n.260-63530G>T
ENST00000525819.1:c.110-17809G>T	ENSP00000434599.1:n.110-17809G>T
ENST00000529324.5:c.110-17809G>T	ENSP00000431619.1:n.110-17809G>T
NM_000944.4:c.260-17809G>T	NP_000935.1:n.260-17809G>T
NM_001130691.1:c.260-17809G>T	NP_001124163.1:n.260-17809G>T
NM_001130692.1:c.260-17809G>T	NP_001124164.1:n.260-17809G>T
XM_017008365.1:c.224-17809G>T	XP_016863854.1:n.224-17809G>T
XM_024454127.1:c.110-17809G>T	XP_024309895.1:n.110-17809G>T
NM_000944.5:c.260-17809G>T MANE Select	NP_000935.1:n.260-17809G>T
NM_001130691.2:c.260-17809G>T	NP_001124163.1:n.260-17809G>T
NM_001130692.2:c.260-17809G>T	NP_001124164.1:n.260-17809G>T