Canonical Allele Identifier: CA407412058

Gene: PRKCG

Linked Data

• MyVariant Identifiers: chr19:g.54385860T>G (hg19) ; chr19:g.53882606T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882606T>G , CM000681.2:g.53882606T>G	GRCh38
NC_000019.9:g.54385860T>G , CM000681.1:g.54385860T>G	GRCh37
NC_000019.8:g.59077672T>G	NCBI36
NG_009114.1:g.5394T>G , LRG_669:g.5394T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.112T>G	ENSP00000507230.1:p.Phe38Val
ENST00000682268.1:n.410T>G
ENST00000682902.1:n.414T>G
ENST00000683513.1:c.112T>G	ENSP00000506809.1:p.Phe38Val
ENST00000263431.4:c.112T>G MANE Select	ENSP00000263431.3:p.Phe38Val
ENST00000263431.3:c.112T>G	ENSP00000263431.3:p.Phe38Val
ENST00000419486.1:c.-273T>G	ENSP00000387919.2:n.-273T>G
ENST00000474397.5:c.-273T>G	ENSP00000471271.1:n.-273T>G
ENST00000479081.5:c.-273T>G	ENSP00000471544.1:n.-273T>G
NM_001316329.1:c.112T>G	NP_001303258.1:p.Phe38Val
NM_002739.3:c.112T>G , LRG_669t1:c.112T>G	NP_002730.1:p.Phe38Val
NM_002739.4:c.112T>G	NP_002730.1:p.Phe38Val
NM_002739.5:c.112T>G MANE Select	NP_002730.1:p.Phe38Val
NM_001316329.2:c.112T>G	NP_001303258.1:p.Phe38Val