Canonical Allele Identifier: CA2814830675

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890060_53890061insTG , CM000681.2:g.53890060_53890061insTG	GRCh38
NC_000019.9:g.54393314_54393315insTG , CM000681.1:g.54393314_54393315insTG	GRCh37
NC_000019.8:g.59085126_59085127insTG	NCBI36
NG_009114.1:g.12848_12849insTG , LRG_669:g.12848_12849insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+43_529+44insTG	ENSP00000507230.1:n.529+43_529+44insTG
ENST00000682268.1:n.827+43_827+44insTG
ENST00000682902.1:n.831+43_831+44insTG
ENST00000683513.1:c.529+43_529+44insTG	ENSP00000506809.1:n.529+43_529+44insTG
ENST00000263431.4:c.529+43_529+44insTG MANE Select	ENSP00000263431.3:n.529+43_529+44insTG
ENST00000263431.3:c.529+43_529+44insTG	ENSP00000263431.3:n.529+43_529+44insTG
ENST00000474397.5:c.145+43_145+44insTG	ENSP00000471271.1:n.145+43_145+44insTG
NM_001316329.1:c.529+43_529+44insTG	NP_001303258.1:n.529+43_529+44insTG
NM_002739.3:c.529+43_529+44insTG , LRG_669t1:c.529+43_529+44insTG	NP_002730.1:n.529+43_529+44insTG
NM_002739.4:c.529+43_529+44insTG	NP_002730.1:n.529+43_529+44insTG
NM_002739.5:c.529+43_529+44insTG MANE Select	NP_002730.1:n.529+43_529+44insTG
NM_001316329.2:c.529+43_529+44insTG	NP_001303258.1:n.529+43_529+44insTG