Canonical Allele Identifier: CA9640564

Gene: PRKCG

Linked Data

• dbSNP Id: rs141380971
• ExAC: 19:54403519 C / G
• gnomAD v2: 19-54403519-C-G
• gnomAD v3: 19-53900265-C-G
• gnomAD v4: 19-53900265-C-G
• MyVariant Identifiers: chr19:g.54403519C>G (hg19) ; chr19:g.53900265C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900265C>G , CM000681.2:g.53900265C>G	GRCh38
NC_000019.9:g.54403519C>G , CM000681.1:g.54403519C>G	GRCh37
NC_000019.8:g.59095331C>G	NCBI36
NG_009114.1:g.23053C>G , LRG_669:g.23053C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1314C>G	ENSP00000507230.1:p.Thr438=
ENST00000682268.1:n.1612C>G
ENST00000682676.1:n.715C>G
ENST00000682902.1:n.1616C>G
ENST00000683513.1:c.1314C>G	ENSP00000506809.1:p.Thr438=
ENST00000263431.4:c.1314C>G MANE Select	ENSP00000263431.3:p.Thr438=
ENST00000263431.3:c.1314C>G	ENSP00000263431.3:p.Thr438=
NM_001316329.1:c.1314C>G	NP_001303258.1:p.Thr438=
NM_002739.3:c.1314C>G , LRG_669t1:c.1314C>G	NP_002730.1:p.Thr438=
NM_002739.4:c.1314C>G	NP_002730.1:p.Thr438=
XM_011527108.1:c.405C>G	XP_011525410.1:p.Thr135=
NM_002739.5:c.1314C>G MANE Select	NP_002730.1:p.Thr438=
NM_001316329.2:c.1314C>G	NP_001303258.1:p.Thr438=