Canonical Allele Identifier: CA310078882

Gene: PRKCG

Linked Data

• dbSNP Id: rs994248167
• gnomAD v3: 19-53882339-T-A
• gnomAD v4: 19-53882339-T-A
• MyVariant Identifiers: chr19:g.54385593T>A (hg19) ; chr19:g.53882339T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882339T>A , CM000681.2:g.53882339T>A	GRCh38
NC_000019.9:g.54385593T>A , CM000681.1:g.54385593T>A	GRCh37
NC_000019.8:g.59077405T>A	NCBI36
NG_009114.1:g.5127T>A , LRG_669:g.5127T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-156T>A	ENSP00000507230.1:n.-156T>A
ENST00000682268.1:n.143T>A
ENST00000682902.1:n.147T>A
ENST00000683513.1:c.-156T>A	ENSP00000506809.1:n.-156T>A
ENST00000263431.4:c.-156T>A MANE Select	ENSP00000263431.3:n.-156T>A
ENST00000263431.3:c.-156T>A	ENSP00000263431.3:n.-156T>A
ENST00000419486.1:c.-343T>A	ENSP00000387919.2:n.-343T>A
ENST00000474397.5:c.-322-218T>A	ENSP00000471271.1:n.-322-218T>A
ENST00000479081.5:c.-322-218T>A	ENSP00000471544.1:n.-322-218T>A
NM_001316329.1:c.-156T>A	NP_001303258.1:n.-156T>A
NM_002739.3:c.-156T>A , LRG_669t1:c.-156T>A	NP_002730.1:n.-156T>A
NM_002739.4:c.-156T>A	NP_002730.1:n.-156T>A
NM_002739.5:c.-156T>A MANE Select	NP_002730.1:n.-156T>A
NM_001316329.2:c.-156T>A	NP_001303258.1:n.-156T>A