Canonical Allele Identifier: CA633841441

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068758661
• gnomAD v2: 19-54404137-C-CGACT
• gnomAD v3: 19-53900883-C-CGACT
• gnomAD v4: 19-53900883-C-CGACT
• MyVariant Identifiers: chr19:g.54404137_54404138insGACT (hg19) ; chr19:g.53900883_53900884insGACT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900884_53900885insACTG , CM000681.2:g.53900884_53900885insACTG	GRCh38
NC_000019.9:g.54404138_54404139insACTG , CM000681.1:g.54404138_54404139insACTG	GRCh37
NC_000019.8:g.59095950_59095951insACTG	NCBI36
NG_009114.1:g.23672_23673insACTG , LRG_669:g.23672_23673insACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+135_1575+136insACTG	ENSP00000507230.1:n.1575+135_1575+136insACTG
ENST00000682268.1:n.1873+135_1873+136insACTG
ENST00000682676.1:n.976+135_976+136insACTG
ENST00000682902.1:n.1877+135_1877+136insACTG
ENST00000683513.1:c.1575+135_1575+136insACTG	ENSP00000506809.1:n.1575+135_1575+136insACTG
ENST00000263431.4:c.1575+135_1575+136insACTG MANE Select	ENSP00000263431.3:n.1575+135_1575+136insACTG
ENST00000263431.3:c.1575+135_1575+136insACTG	ENSP00000263431.3:n.1575+135_1575+136insACTG
NM_001316329.1:c.1575+135_1575+136insACTG	NP_001303258.1:n.1575+135_1575+136insACTG
NM_002739.3:c.1575+135_1575+136insACTG , LRG_669t1:c.1575+135_1575+136insACTG	NP_002730.1:n.1575+135_1575+136insACTG
NM_002739.4:c.1575+135_1575+136insACTG	NP_002730.1:n.1575+135_1575+136insACTG
XM_011527108.1:c.666+135_666+136insACTG	XP_011525410.1:n.666+135_666+136insACTG
NM_002739.5:c.1575+135_1575+136insACTG MANE Select	NP_002730.1:n.1575+135_1575+136insACTG
NM_001316329.2:c.1575+135_1575+136insACTG	NP_001303258.1:n.1575+135_1575+136insACTG