Canonical Allele Identifier: CA407418937

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 994941
• ClinVar RCV Id: RCV001288721
• dbSNP Id: rs2068757477
• MyVariant Identifiers: chr19:g.54403981C>T (hg19) ; chr19:g.53900727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900727C>T , CM000681.2:g.53900727C>T	GRCh38
NC_000019.9:g.54403981C>T , CM000681.1:g.54403981C>T	GRCh37
NC_000019.8:g.59095793C>T	NCBI36
NG_009114.1:g.23515C>T , LRG_669:g.23515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1553C>T	ENSP00000507230.1:p.Thr518Ile
ENST00000682268.1:n.1851C>T
ENST00000682676.1:n.954C>T
ENST00000682902.1:n.1855C>T
ENST00000683513.1:c.1553C>T	ENSP00000506809.1:p.Thr518Ile
ENST00000263431.4:c.1553C>T MANE Select	ENSP00000263431.3:p.Thr518Ile
ENST00000263431.3:c.1553C>T	ENSP00000263431.3:p.Thr518Ile
NM_001316329.1:c.1553C>T	NP_001303258.1:p.Thr518Ile
NM_002739.3:c.1553C>T , LRG_669t1:c.1553C>T	NP_002730.1:p.Thr518Ile
NM_002739.4:c.1553C>T	NP_002730.1:p.Thr518Ile
XM_011527108.1:c.644C>T	XP_011525410.1:p.Thr215Ile
NM_002739.5:c.1553C>T MANE Select	NP_002730.1:p.Thr518Ile
NM_001316329.2:c.1553C>T	NP_001303258.1:p.Thr518Ile