Canonical Allele Identifier: CA2586974996

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900313-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900317del , CM000681.2:g.53900317del	GRCh38
NC_000019.9:g.54403571del , CM000681.1:g.54403571del	GRCh37
NC_000019.8:g.59095383del	NCBI36
NG_009114.1:g.23105del , LRG_669:g.23105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1366del	ENSP00000507230.1:p.His456MetfsTer26
ENST00000682268.1:n.1664del
ENST00000682676.1:n.767del
ENST00000682902.1:n.1668del
ENST00000683513.1:c.1366del	ENSP00000506809.1:p.His456MetfsTer26
ENST00000263431.4:c.1366del MANE Select	ENSP00000263431.3:p.His456MetfsTer26
ENST00000263431.3:c.1366del	ENSP00000263431.3:p.His456MetfsTer26
NM_001316329.1:c.1366del	NP_001303258.1:p.His456MetfsTer26
NM_002739.3:c.1366del , LRG_669t1:c.1366del	NP_002730.1:p.His456MetfsTer26
NM_002739.4:c.1366del	NP_002730.1:p.His456MetfsTer26
XM_011527108.1:c.457del	XP_011525410.1:p.His153MetfsTer26
NM_002739.5:c.1366del MANE Select	NP_002730.1:p.His456MetfsTer26
NM_001316329.2:c.1366del	NP_001303258.1:p.His456MetfsTer26