Canonical Allele Identifier: CA2342579491

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068662278

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890084A>T , CM000681.2:g.53890084A>T	GRCh38
NC_000019.9:g.54393338A>T , CM000681.1:g.54393338A>T	GRCh37
NC_000019.8:g.59085150A>T	NCBI36
NG_009114.1:g.12872A>T , LRG_669:g.12872A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+67A>T	ENSP00000507230.1:n.529+67A>T
ENST00000682268.1:n.827+67A>T
ENST00000682902.1:n.831+67A>T
ENST00000683513.1:c.529+67A>T	ENSP00000506809.1:n.529+67A>T
ENST00000263431.4:c.529+67A>T MANE Select	ENSP00000263431.3:n.529+67A>T
ENST00000263431.3:c.529+67A>T	ENSP00000263431.3:n.529+67A>T
ENST00000474397.5:c.145+67A>T	ENSP00000471271.1:n.145+67A>T
NM_001316329.1:c.529+67A>T	NP_001303258.1:n.529+67A>T
NM_002739.3:c.529+67A>T , LRG_669t1:c.529+67A>T	NP_002730.1:n.529+67A>T
NM_002739.4:c.529+67A>T	NP_002730.1:n.529+67A>T
NM_002739.5:c.529+67A>T MANE Select	NP_002730.1:n.529+67A>T
NM_001316329.2:c.529+67A>T	NP_001303258.1:n.529+67A>T