Canonical Allele Identifier: CA633905648

Gene: PRKCG

Linked Data

• dbSNP Id: rs1304543827
• gnomAD v2: 19-54385740-T-G
• gnomAD v3: 19-53882486-T-G
• gnomAD v4: 19-53882486-T-G
• MyVariant Identifiers: chr19:g.54385740T>G (hg19) ; chr19:g.53882486T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882486T>G , CM000681.2:g.53882486T>G	GRCh38
NC_000019.9:g.54385740T>G , CM000681.1:g.54385740T>G	GRCh37
NC_000019.8:g.59077552T>G	NCBI36
NG_009114.1:g.5274T>G , LRG_669:g.5274T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-9T>G	ENSP00000507230.1:n.-9T>G
ENST00000682268.1:n.290T>G
ENST00000682902.1:n.294T>G
ENST00000683513.1:c.-9T>G	ENSP00000506809.1:n.-9T>G
ENST00000263431.4:c.-9T>G MANE Select	ENSP00000263431.3:n.-9T>G
ENST00000263431.3:c.-9T>G	ENSP00000263431.3:n.-9T>G
ENST00000419486.1:c.-322-71T>G	ENSP00000387919.2:n.-322-71T>G
ENST00000474397.5:c.-322-71T>G	ENSP00000471271.1:n.-322-71T>G
ENST00000479081.5:c.-322-71T>G	ENSP00000471544.1:n.-322-71T>G
NM_001316329.1:c.-9T>G	NP_001303258.1:n.-9T>G
NM_002739.3:c.-9T>G , LRG_669t1:c.-9T>G	NP_002730.1:n.-9T>G
NM_002739.4:c.-9T>G	NP_002730.1:n.-9T>G
NM_002739.5:c.-9T>G MANE Select	NP_002730.1:n.-9T>G
NM_001316329.2:c.-9T>G	NP_001303258.1:n.-9T>G