Canonical Allele Identifier: CA9640317

Gene: PRKCG

Linked Data

• dbSNP Id: rs751456549
• ExAC: 19:54393322 G / GGGGCTGACCCAAGGCACTT
• gnomAD v2: 19-54393322-G-GGGGCTGACCCAAGGCACTT
• gnomAD v3: 19-53890068-G-GGGGCTGACCCAAGGCACTT
• gnomAD v4: 19-53890068-G-GGGGCTGACCCAAGGCACTT
• MyVariant Identifiers: chr19:g.54393322_54393323insGGGCTGACCCAAGGCACTT (hg19) ; chr19:g.53890068_53890069insGGGCTGACCCAAGGCACTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890070_53890088dup , CM000681.2:g.53890070_53890088dup	GRCh38
NC_000019.9:g.54393324_54393342dup , CM000681.1:g.54393324_54393342dup	GRCh37
NC_000019.8:g.59085136_59085154dup	NCBI36
NG_009114.1:g.12858_12876dup , LRG_669:g.12858_12876dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+53_529+71dup	ENSP00000507230.1:n.529+53_529+71dup
ENST00000682268.1:n.827+53_827+71dup
ENST00000682902.1:n.831+53_831+71dup
ENST00000683513.1:c.529+53_529+71dup	ENSP00000506809.1:n.529+53_529+71dup
ENST00000263431.4:c.529+53_529+71dup MANE Select	ENSP00000263431.3:n.529+53_529+71dup
ENST00000263431.3:c.529+53_529+71dup	ENSP00000263431.3:n.529+53_529+71dup
ENST00000474397.5:c.145+53_145+71dup	ENSP00000471271.1:n.145+53_145+71dup
NM_001316329.1:c.529+53_529+71dup	NP_001303258.1:n.529+53_529+71dup
NM_002739.3:c.529+53_529+71dup , LRG_669t1:c.529+53_529+71dup	NP_002730.1:n.529+53_529+71dup
NM_002739.4:c.529+53_529+71dup	NP_002730.1:n.529+53_529+71dup
NM_002739.5:c.529+53_529+71dup MANE Select	NP_002730.1:n.529+53_529+71dup
NM_001316329.2:c.529+53_529+71dup	NP_001303258.1:n.529+53_529+71dup