Canonical Allele Identifier: CA407417369

Gene: PRKCG

Linked Data

• gnomAD v3: 19-53897998-C-G
• gnomAD v4: 19-53897998-C-G
• MyVariant Identifiers: chr19:g.54401252C>G (hg19) ; chr19:g.53897998C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53897998C>G , CM000681.2:g.53897998C>G	GRCh38
NC_000019.9:g.54401252C>G , CM000681.1:g.54401252C>G	GRCh37
NC_000019.8:g.59093064C>G	NCBI36
NG_009114.1:g.20786C>G , LRG_669:g.20786C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.979C>G	ENSP00000507230.1:p.Pro327Ala
ENST00000682268.1:n.1277C>G
ENST00000682676.1:n.380C>G
ENST00000682902.1:n.1281C>G
ENST00000683513.1:c.979C>G	ENSP00000506809.1:p.Pro327Ala
ENST00000263431.4:c.979C>G MANE Select	ENSP00000263431.3:p.Pro327Ala
ENST00000263431.3:c.979C>G	ENSP00000263431.3:p.Pro327Ala
NM_001316329.1:c.979C>G	NP_001303258.1:p.Pro327Ala
NM_002739.3:c.979C>G , LRG_669t1:c.979C>G	NP_002730.1:p.Pro327Ala
NM_002739.4:c.979C>G	NP_002730.1:p.Pro327Ala
XM_011527108.1:c.70C>G	XP_011525410.1:p.Pro24Ala
NM_002739.5:c.979C>G MANE Select	NP_002730.1:p.Pro327Ala
NM_001316329.2:c.979C>G	NP_001303258.1:p.Pro327Ala