Canonical Allele Identifier: CA9640307

Gene: PRKCG

Linked Data

• dbSNP Id: rs762986495
• ExAC: 19:54393275 AGGCCCCGCCCCCTCGCCT / A
• gnomAD v2: 19-54393275-AGGCCCCGCCCCCTCGCCT-A
• gnomAD v3: 19-53890021-AGGCCCCGCCCCCTCGCCT-A
• gnomAD v4: 19-53890021-AGGCCCCGCCCCCTCGCCT-A
• MyVariant Identifiers: chr19:g.54393276_54393293del (hg19) ; chr19:g.53890022_53890039del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890036_53890053del , CM000681.2:g.53890036_53890053del	GRCh38
NC_000019.9:g.54393290_54393307del , CM000681.1:g.54393290_54393307del	GRCh37
NC_000019.8:g.59085102_59085119del	NCBI36
NG_009114.1:g.12824_12841del , LRG_669:g.12824_12841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+19_529+36del	ENSP00000507230.1:n.529+19_529+36del
ENST00000682268.1:n.827+19_827+36del
ENST00000682902.1:n.831+19_831+36del
ENST00000683513.1:c.529+19_529+36del	ENSP00000506809.1:n.529+19_529+36del
ENST00000263431.4:c.529+19_529+36del MANE Select	ENSP00000263431.3:n.529+19_529+36del
ENST00000263431.3:c.529+19_529+36del	ENSP00000263431.3:n.529+19_529+36del
ENST00000474397.5:c.145+19_145+36del	ENSP00000471271.1:n.145+19_145+36del
NM_001316329.1:c.529+19_529+36del	NP_001303258.1:n.529+19_529+36del
NM_002739.3:c.529+19_529+36del , LRG_669t1:c.529+19_529+36del	NP_002730.1:n.529+19_529+36del
NM_002739.4:c.529+19_529+36del	NP_002730.1:n.529+19_529+36del
NM_002739.5:c.529+19_529+36del MANE Select	NP_002730.1:n.529+19_529+36del
NM_001316329.2:c.529+19_529+36del	NP_001303258.1:n.529+19_529+36del