Canonical Allele Identifier: CA633905659

Gene: PRKCG

Linked Data

• dbSNP Id: rs781474547
• gnomAD v2: 19-54403619-G-T
• gnomAD v3: 19-53900365-G-T
• gnomAD v4: 19-53900365-G-T
• MyVariant Identifiers: chr19:g.54403619G>T (hg19) ; chr19:g.53900365G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900365G>T , CM000681.2:g.53900365G>T	GRCh38
NC_000019.9:g.54403619G>T , CM000681.1:g.54403619G>T	GRCh37
NC_000019.8:g.59095431G>T	NCBI36
NG_009114.1:g.23153G>T , LRG_669:g.23153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1373+41G>T	ENSP00000507230.1:n.1373+41G>T
ENST00000682268.1:n.1671+41G>T
ENST00000682676.1:n.774+41G>T
ENST00000682902.1:n.1675+41G>T
ENST00000683513.1:c.1373+41G>T	ENSP00000506809.1:n.1373+41G>T
ENST00000263431.4:c.1373+41G>T MANE Select	ENSP00000263431.3:n.1373+41G>T
ENST00000263431.3:c.1373+41G>T	ENSP00000263431.3:n.1373+41G>T
NM_001316329.1:c.1373+41G>T	NP_001303258.1:n.1373+41G>T
NM_002739.3:c.1373+41G>T , LRG_669t1:c.1373+41G>T	NP_002730.1:n.1373+41G>T
NM_002739.4:c.1373+41G>T	NP_002730.1:n.1373+41G>T
XM_011527108.1:c.464+41G>T	XP_011525410.1:n.464+41G>T
NM_002739.5:c.1373+41G>T MANE Select	NP_002730.1:n.1373+41G>T
NM_001316329.2:c.1373+41G>T	NP_001303258.1:n.1373+41G>T