Canonical Allele Identifier: CA154782

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 130037
• ClinVar RCV Id: RCV000118063 ; RCV000611784 ; RCV000992824
• dbSNP Id: rs2547362
• ExAC: 19:54385820 C / T
• gnomAD v2: 19-54385820-C-T
• gnomAD v3: 19-53882566-C-T
• gnomAD v4: 19-53882566-C-T
• MyVariant Identifiers: chr19:g.54385820C>T (hg19) ; chr19:g.53882566C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882566C>T , CM000681.2:g.53882566C>T	GRCh38
NC_000019.9:g.54385820C>T , CM000681.1:g.54385820C>T	GRCh37
NC_000019.8:g.59077632C>T	NCBI36
NG_009114.1:g.5354C>T , LRG_669:g.5354C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.72C>T	ENSP00000507230.1:p.Ala24=
ENST00000682268.1:n.370C>T
ENST00000682902.1:n.374C>T
ENST00000683513.1:c.72C>T	ENSP00000506809.1:p.Ala24=
ENST00000263431.4:c.72C>T MANE Select	ENSP00000263431.3:p.Ala24=
ENST00000263431.3:c.72C>T	ENSP00000263431.3:p.Ala24=
ENST00000419486.1:c.-313C>T	ENSP00000387919.2:n.-313C>T
ENST00000474397.5:c.-313C>T	ENSP00000471271.1:n.-313C>T
ENST00000479081.5:c.-313C>T	ENSP00000471544.1:n.-313C>T
NM_001316329.1:c.72C>T	NP_001303258.1:p.Ala24=
NM_002739.3:c.72C>T , LRG_669t1:c.72C>T	NP_002730.1:p.Ala24=
NM_002739.4:c.72C>T	NP_002730.1:p.Ala24=
NM_002739.5:c.72C>T MANE Select	NP_002730.1:p.Ala24=
NM_001316329.2:c.72C>T	NP_001303258.1:p.Ala24=