Canonical Allele Identifier: CA1651290

Gene: PPP1R21

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48486638C>T , CM000664.2:g.48486638C>T	GRCh38
NC_000002.11:g.48713777C>T , CM000664.1:g.48713777C>T	GRCh37
NC_000002.10:g.48567281C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294952.13:c.1326C>T MANE Select	ENSP00000294952.8:p.Ser442=
ENST00000281394.8:c.1326C>T	ENSP00000281394.4:p.Ser442=
ENST00000294952.12:c.1326C>T	ENSP00000294952.8:p.Ser442=
ENST00000416913.5:c.*1200C>T	ENSP00000414130.1:n.*1200C>T
ENST00000431614.5:c.*1150C>T	ENSP00000406283.1:n.*1150C>T
ENST00000449090.6:c.1326C>T	ENSP00000415696.2:p.Ser442=
ENST00000455978.1:c.368C>T
NM_001135629.2:c.1326C>T	NP_001129101.1:p.Ser442=
NM_001193475.1:c.1326C>T	NP_001180404.1:p.Ser442=
NM_152994.4:c.1326C>T	NP_694539.1:p.Ser442=
NR_024188.2:n.1550C>T
XR_939654.1:n.1479C>T
XR_939655.1:n.1552C>T
XM_017003301.1:c.831C>T	XP_016858790.1:p.Ser277=
XM_017003302.1:c.831C>T	XP_016858791.1:p.Ser277=
XR_001738608.1:n.1479C>T
XR_001738609.1:n.1552C>T
NM_001135629.3:c.1326C>T MANE Select	NP_001129101.1:p.Ser442=
NM_152994.5:c.1326C>T	NP_694539.1:p.Ser442=
NR_024188.3:n.1553C>T
NM_001193475.2:c.1326C>T	NP_001180404.1:p.Ser442=