Canonical Allele Identifier: CA633905565

Gene: PRKCG

Linked Data

• dbSNP Id: rs1159681689
• gnomAD v2: 19-54385483-ACCG-A
• gnomAD v4: 19-53882229-ACCG-A
• MyVariant Identifiers: chr19:g.54385484_54385486del (hg19) ; chr19:g.53882230_53882232del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882238_53882240del , CM000681.2:g.53882238_53882240del	GRCh38
NC_000019.9:g.54385492_54385494del , CM000681.1:g.54385492_54385494del	GRCh37
NC_000019.8:g.59077304_59077306del	NCBI36
NG_009114.1:g.5026_5028del , LRG_669:g.5026_5028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-257_-255del	ENSP00000507230.1:n.-257_-255del
ENST00000682268.1:n.42_44del
ENST00000682902.1:n.46_48del
ENST00000683513.1:c.-257_-255del	ENSP00000506809.1:n.-257_-255del
ENST00000263431.4:c.-257_-255del MANE Select	ENSP00000263431.3:n.-257_-255del
ENST00000263431.3:c.-257_-255del	ENSP00000263431.3:n.-257_-255del
ENST00000419486.1:c.-444_-442del	ENSP00000387919.2:n.-444_-442del
ENST00000474397.5:c.-322-319_-322-317del	ENSP00000471271.1:n.-322-319_-322-317del
ENST00000479081.5:c.-322-319_-322-317del	ENSP00000471544.1:n.-322-319_-322-317del
NM_001316329.1:c.-257_-255del	NP_001303258.1:n.-257_-255del
NM_002739.3:c.-257_-255del , LRG_669t1:c.-257_-255del	NP_002730.1:n.-257_-255del
NM_002739.4:c.-257_-255del	NP_002730.1:n.-257_-255del
NM_002739.5:c.-257_-255del MANE Select	NP_002730.1:n.-257_-255del
NM_001316329.2:c.-257_-255del	NP_001303258.1:n.-257_-255del