Canonical Allele Identifier: CA407418335

Gene: PRKCG

Linked Data

• dbSNP Id: rs1311765439
• gnomAD v2: 19-54403538-C-A
• gnomAD v4: 19-53900284-C-A
• MyVariant Identifiers: chr19:g.54403538C>A (hg19) ; chr19:g.53900284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900284C>A , CM000681.2:g.53900284C>A	GRCh38
NC_000019.9:g.54403538C>A , CM000681.1:g.54403538C>A	GRCh37
NC_000019.8:g.59095350C>A	NCBI36
NG_009114.1:g.23072C>A , LRG_669:g.23072C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1333C>A	ENSP00000507230.1:p.His445Asn
ENST00000682268.1:n.1631C>A
ENST00000682676.1:n.734C>A
ENST00000682902.1:n.1635C>A
ENST00000683513.1:c.1333C>A	ENSP00000506809.1:p.His445Asn
ENST00000263431.4:c.1333C>A MANE Select	ENSP00000263431.3:p.His445Asn
ENST00000263431.3:c.1333C>A	ENSP00000263431.3:p.His445Asn
NM_001316329.1:c.1333C>A	NP_001303258.1:p.His445Asn
NM_002739.3:c.1333C>A , LRG_669t1:c.1333C>A	NP_002730.1:p.His445Asn
NM_002739.4:c.1333C>A	NP_002730.1:p.His445Asn
XM_011527108.1:c.424C>A	XP_011525410.1:p.His142Asn
NM_002739.5:c.1333C>A MANE Select	NP_002730.1:p.His445Asn
NM_001316329.2:c.1333C>A	NP_001303258.1:p.His445Asn