Canonical Allele Identifier: CA633905599

Gene: PRKCG

Linked Data

• dbSNP Id: rs1230895829
• gnomAD v2: 19-54385577-G-T
• gnomAD v4: 19-53882323-G-T
• MyVariant Identifiers: chr19:g.54385577G>T (hg19) ; chr19:g.53882323G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882323G>T , CM000681.2:g.53882323G>T	GRCh38
NC_000019.9:g.54385577G>T , CM000681.1:g.54385577G>T	GRCh37
NC_000019.8:g.59077389G>T	NCBI36
NG_009114.1:g.5111G>T , LRG_669:g.5111G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-172G>T	ENSP00000507230.1:n.-172G>T
ENST00000682268.1:n.127G>T
ENST00000682902.1:n.131G>T
ENST00000683513.1:c.-172G>T	ENSP00000506809.1:n.-172G>T
ENST00000263431.4:c.-172G>T MANE Select	ENSP00000263431.3:n.-172G>T
ENST00000263431.3:c.-172G>T	ENSP00000263431.3:n.-172G>T
ENST00000419486.1:c.-359G>T	ENSP00000387919.2:n.-359G>T
ENST00000474397.5:c.-322-234G>T	ENSP00000471271.1:n.-322-234G>T
ENST00000479081.5:c.-322-234G>T	ENSP00000471544.1:n.-322-234G>T
NM_001316329.1:c.-172G>T	NP_001303258.1:n.-172G>T
NM_002739.3:c.-172G>T , LRG_669t1:c.-172G>T	NP_002730.1:n.-172G>T
NM_002739.4:c.-172G>T	NP_002730.1:n.-172G>T
NM_002739.5:c.-172G>T MANE Select	NP_002730.1:n.-172G>T
NM_001316329.2:c.-172G>T	NP_001303258.1:n.-172G>T