Canonical Allele Identifier: CA2582263417

Gene: PRKCG

Linked Data

• gnomAD v3: 19-53900265-C-CG
• gnomAD v4: 19-53900265-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900270dup , CM000681.2:g.53900270dup	GRCh38
NC_000019.9:g.54403524dup , CM000681.1:g.54403524dup	GRCh37
NC_000019.8:g.59095336dup	NCBI36
NG_009114.1:g.23058dup , LRG_669:g.23058dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1319dup	ENSP00000507230.1:p.Asp441ArgfsTer13
ENST00000682268.1:n.1617dup
ENST00000682676.1:n.720dup
ENST00000682902.1:n.1621dup
ENST00000683513.1:c.1319dup	ENSP00000506809.1:p.Asp441ArgfsTer13
ENST00000263431.4:c.1319dup MANE Select	ENSP00000263431.3:p.Asp441ArgfsTer13
ENST00000263431.3:c.1319dup	ENSP00000263431.3:p.Asp441ArgfsTer13
NM_001316329.1:c.1319dup	NP_001303258.1:p.Asp441ArgfsTer13
NM_002739.3:c.1319dup , LRG_669t1:c.1319dup	NP_002730.1:p.Asp441ArgfsTer13
NM_002739.4:c.1319dup	NP_002730.1:p.Asp441ArgfsTer13
XM_011527108.1:c.410dup	XP_011525410.1:p.Asp138ArgfsTer13
NM_002739.5:c.1319dup MANE Select	NP_002730.1:p.Asp441ArgfsTer13
NM_001316329.2:c.1319dup	NP_001303258.1:p.Asp441ArgfsTer13