Canonical Allele Identifier: CA310092491

Gene: PRKCG

Linked Data

• dbSNP Id: rs891265577
• MyVariant Identifiers: chr19:g.54404171A>G (hg19) ; chr19:g.53900917A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900917A>G , CM000681.2:g.53900917A>G	GRCh38
NC_000019.9:g.54404171A>G , CM000681.1:g.54404171A>G	GRCh37
NC_000019.8:g.59095983A>G	NCBI36
NG_009114.1:g.23705A>G , LRG_669:g.23705A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+168A>G	ENSP00000507230.1:n.1575+168A>G
ENST00000682268.1:n.1873+168A>G
ENST00000682676.1:n.976+168A>G
ENST00000682902.1:n.1877+168A>G
ENST00000683513.1:c.1575+168A>G	ENSP00000506809.1:n.1575+168A>G
ENST00000263431.4:c.1575+168A>G MANE Select	ENSP00000263431.3:n.1575+168A>G
ENST00000263431.3:c.1575+168A>G	ENSP00000263431.3:n.1575+168A>G
NM_001316329.1:c.1575+168A>G	NP_001303258.1:n.1575+168A>G
NM_002739.3:c.1575+168A>G , LRG_669t1:c.1575+168A>G	NP_002730.1:n.1575+168A>G
NM_002739.4:c.1575+168A>G	NP_002730.1:n.1575+168A>G
XM_011527108.1:c.666+168A>G	XP_011525410.1:n.666+168A>G
NM_002739.5:c.1575+168A>G MANE Select	NP_002730.1:n.1575+168A>G
NM_001316329.2:c.1575+168A>G	NP_001303258.1:n.1575+168A>G