Canonical Allele Identifier: CA2586963504

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53890113-A-AGGCGTGGCCCCATCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890113_53890114insGGCGTGGCCCCATCTT , CM000681.2:g.53890113_53890114insGGCGTGGCCCCATCTT	GRCh38
NC_000019.9:g.54393367_54393368insGGCGTGGCCCCATCTT , CM000681.1:g.54393367_54393368insGGCGTGGCCCCATCTT	GRCh37
NC_000019.8:g.59085179_59085180insGGCGTGGCCCCATCTT	NCBI36
NG_009114.1:g.12901_12902insGGCGTGGCCCCATCTT , LRG_669:g.12901_12902insGGCGTGGCCCCATCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+96_529+97insGGCGTGGCCCCATCTT	ENSP00000507230.1:n.529+96_529+97insGGCGTGGCCCCATCTT
ENST00000682268.1:n.827+96_827+97insGGCGTGGCCCCATCTT
ENST00000682902.1:n.831+96_831+97insGGCGTGGCCCCATCTT
ENST00000683513.1:c.529+96_529+97insGGCGTGGCCCCATCTT	ENSP00000506809.1:n.529+96_529+97insGGCGTGGCCCCATCTT
ENST00000263431.4:c.529+96_529+97insGGCGTGGCCCCATCTT MANE Select	ENSP00000263431.3:n.529+96_529+97insGGCGTGGCCCCATCTT
ENST00000263431.3:c.529+96_529+97insGGCGTGGCCCCATCTT	ENSP00000263431.3:n.529+96_529+97insGGCGTGGCCCCATCTT
ENST00000474397.5:c.145+96_145+97insGGCGTGGCCCCATCTT	ENSP00000471271.1:n.145+96_145+97insGGCGTGGCCCCATCTT
NM_001316329.1:c.529+96_529+97insGGCGTGGCCCCATCTT	NP_001303258.1:n.529+96_529+97insGGCGTGGCCCCATCTT
NM_002739.3:c.529+96_529+97insGGCGTGGCCCCATCTT , LRG_669t1:c.529+96_529+97insGGCGTGGCCCCATCTT	NP_002730.1:n.529+96_529+97insGGCGTGGCCCCATCTT
NM_002739.4:c.529+96_529+97insGGCGTGGCCCCATCTT	NP_002730.1:n.529+96_529+97insGGCGTGGCCCCATCTT
NM_002739.5:c.529+96_529+97insGGCGTGGCCCCATCTT MANE Select	NP_002730.1:n.529+96_529+97insGGCGTGGCCCCATCTT
NM_001316329.2:c.529+96_529+97insGGCGTGGCCCCATCTT	NP_001303258.1:n.529+96_529+97insGGCGTGGCCCCATCTT