Canonical Allele Identifier: CA9640311

Gene: PRKCG

Linked Data

• dbSNP Id: rs911948396
• ExAC: 19:54393290 G / T
• gnomAD v2: 19-54393290-G-T
• gnomAD v3: 19-53890036-G-T
• gnomAD v4: 19-53890036-G-T
• MyVariant Identifiers: chr19:g.54393290G>T (hg19) ; chr19:g.54393290_54393308delinsTCCTGGCCCCGCCCCCTCC (hg19) ; chr19:g.53890036G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890036G>T , CM000681.2:g.53890036G>T	GRCh38
NC_000019.9:g.54393290G>T , CM000681.1:g.54393290G>T	GRCh37
NC_000019.8:g.59085102G>T	NCBI36
NG_009114.1:g.12824G>T , LRG_669:g.12824G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+19G>T	ENSP00000507230.1:n.529+19G>T
ENST00000682268.1:n.827+19G>T
ENST00000682902.1:n.831+19G>T
ENST00000683513.1:c.529+19G>T	ENSP00000506809.1:n.529+19G>T
ENST00000263431.4:c.529+19G>T MANE Select	ENSP00000263431.3:n.529+19G>T
ENST00000263431.3:c.529+19G>T	ENSP00000263431.3:n.529+19G>T
ENST00000474397.5:c.145+19G>T	ENSP00000471271.1:n.145+19G>T
NM_001316329.1:c.529+19G>T	NP_001303258.1:n.529+19G>T
NM_002739.3:c.529+19G>T , LRG_669t1:c.529+19G>T	NP_002730.1:n.529+19G>T
NM_002739.4:c.529+19G>T	NP_002730.1:n.529+19G>T
NM_002739.5:c.529+19G>T MANE Select	NP_002730.1:n.529+19G>T
NM_001316329.2:c.529+19G>T	NP_001303258.1:n.529+19G>T