Canonical Allele Identifier: CA2586963447

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53890060-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890060T>C , CM000681.2:g.53890060T>C	GRCh38
NC_000019.9:g.54393314T>C , CM000681.1:g.54393314T>C	GRCh37
NC_000019.8:g.59085126T>C	NCBI36
NG_009114.1:g.12848T>C , LRG_669:g.12848T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+43T>C	ENSP00000507230.1:n.529+43T>C
ENST00000682268.1:n.827+43T>C
ENST00000682902.1:n.831+43T>C
ENST00000683513.1:c.529+43T>C	ENSP00000506809.1:n.529+43T>C
ENST00000263431.4:c.529+43T>C MANE Select	ENSP00000263431.3:n.529+43T>C
ENST00000263431.3:c.529+43T>C	ENSP00000263431.3:n.529+43T>C
ENST00000474397.5:c.145+43T>C	ENSP00000471271.1:n.145+43T>C
NM_001316329.1:c.529+43T>C	NP_001303258.1:n.529+43T>C
NM_002739.3:c.529+43T>C , LRG_669t1:c.529+43T>C	NP_002730.1:n.529+43T>C
NM_002739.4:c.529+43T>C	NP_002730.1:n.529+43T>C
NM_002739.5:c.529+43T>C MANE Select	NP_002730.1:n.529+43T>C
NM_001316329.2:c.529+43T>C	NP_001303258.1:n.529+43T>C