Canonical Allele Identifier: CA407411929

Gene: PRKCG

Linked Data

• dbSNP Id: rs1599937036
• gnomAD v3: 19-53882579-G-A
• gnomAD v4: 19-53882579-G-A
• MyVariant Identifiers: chr19:g.54385833G>A (hg19) ; chr19:g.53882579G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882579G>A , CM000681.2:g.53882579G>A	GRCh38
NC_000019.9:g.54385833G>A , CM000681.1:g.54385833G>A	GRCh37
NC_000019.8:g.59077645G>A	NCBI36
NG_009114.1:g.5367G>A , LRG_669:g.5367G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.85G>A	ENSP00000507230.1:p.Val29Met
ENST00000682268.1:n.383G>A
ENST00000682902.1:n.387G>A
ENST00000683513.1:c.85G>A	ENSP00000506809.1:p.Val29Met
ENST00000263431.4:c.85G>A MANE Select	ENSP00000263431.3:p.Val29Met
ENST00000263431.3:c.85G>A	ENSP00000263431.3:p.Val29Met
ENST00000419486.1:c.-300G>A	ENSP00000387919.2:n.-300G>A
ENST00000474397.5:c.-300G>A	ENSP00000471271.1:n.-300G>A
ENST00000479081.5:c.-300G>A	ENSP00000471544.1:n.-300G>A
NM_001316329.1:c.85G>A	NP_001303258.1:p.Val29Met
NM_002739.3:c.85G>A , LRG_669t1:c.85G>A	NP_002730.1:p.Val29Met
NM_002739.4:c.85G>A	NP_002730.1:p.Val29Met
NM_002739.5:c.85G>A MANE Select	NP_002730.1:p.Val29Met
NM_001316329.2:c.85G>A	NP_001303258.1:p.Val29Met