Canonical Allele Identifier: CA2586975121

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900865-C-CGA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900865_53900866insGA , CM000681.2:g.53900865_53900866insGA	GRCh38
NC_000019.9:g.54404119_54404120insGA , CM000681.1:g.54404119_54404120insGA	GRCh37
NC_000019.8:g.59095931_59095932insGA	NCBI36
NG_009114.1:g.23653_23654insGA , LRG_669:g.23653_23654insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+116_1575+117insGA	ENSP00000507230.1:n.1575+116_1575+117insGA
ENST00000682268.1:n.1873+116_1873+117insGA
ENST00000682676.1:n.976+116_976+117insGA
ENST00000682902.1:n.1877+116_1877+117insGA
ENST00000683513.1:c.1575+116_1575+117insGA	ENSP00000506809.1:n.1575+116_1575+117insGA
ENST00000263431.4:c.1575+116_1575+117insGA MANE Select	ENSP00000263431.3:n.1575+116_1575+117insGA
ENST00000263431.3:c.1575+116_1575+117insGA	ENSP00000263431.3:n.1575+116_1575+117insGA
NM_001316329.1:c.1575+116_1575+117insGA	NP_001303258.1:n.1575+116_1575+117insGA
NM_002739.3:c.1575+116_1575+117insGA , LRG_669t1:c.1575+116_1575+117insGA	NP_002730.1:n.1575+116_1575+117insGA
NM_002739.4:c.1575+116_1575+117insGA	NP_002730.1:n.1575+116_1575+117insGA
XM_011527108.1:c.666+116_666+117insGA	XP_011525410.1:n.666+116_666+117insGA
NM_002739.5:c.1575+116_1575+117insGA MANE Select	NP_002730.1:n.1575+116_1575+117insGA
NM_001316329.2:c.1575+116_1575+117insGA	NP_001303258.1:n.1575+116_1575+117insGA