Canonical Allele Identifier: CA2586974993

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900259-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900260dup , CM000681.2:g.53900260dup	GRCh38
NC_000019.9:g.54403514dup , CM000681.1:g.54403514dup	GRCh37
NC_000019.8:g.59095326dup	NCBI36
NG_009114.1:g.23048dup , LRG_669:g.23048dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1309dup	ENSP00000507230.1:p.Val437GlyfsTer17
ENST00000682268.1:n.1607dup
ENST00000682676.1:n.710dup
ENST00000682902.1:n.1611dup
ENST00000683513.1:c.1309dup	ENSP00000506809.1:p.Val437GlyfsTer17
ENST00000263431.4:c.1309dup MANE Select	ENSP00000263431.3:p.Val437GlyfsTer17
ENST00000263431.3:c.1309dup	ENSP00000263431.3:p.Val437GlyfsTer17
NM_001316329.1:c.1309dup	NP_001303258.1:p.Val437GlyfsTer17
NM_002739.3:c.1309dup , LRG_669t1:c.1309dup	NP_002730.1:p.Val437GlyfsTer17
NM_002739.4:c.1309dup	NP_002730.1:p.Val437GlyfsTer17
XM_011527108.1:c.400dup	XP_011525410.1:p.Val134GlyfsTer17
NM_002739.5:c.1309dup MANE Select	NP_002730.1:p.Val437GlyfsTer17
NM_001316329.2:c.1309dup	NP_001303258.1:p.Val437GlyfsTer17