Canonical Allele Identifier: CA9640602

Gene: PRKCG

Linked Data

• dbSNP Id: rs754412174
• ExAC: 19:54403697 C / T
• gnomAD v2: 19-54403697-C-T
• gnomAD v4: 19-53900443-C-T
• COSMIC: COSM2929279 ; COSM2929280
• MyVariant Identifiers: chr19:g.54403697C>T (hg19) ; chr19:g.53900443C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900443C>T , CM000681.2:g.53900443C>T	GRCh38
NC_000019.9:g.54403697C>T , CM000681.1:g.54403697C>T	GRCh37
NC_000019.8:g.59095509C>T	NCBI36
NG_009114.1:g.23231C>T , LRG_669:g.23231C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1398C>T	ENSP00000507230.1:p.Ile466=
ENST00000682268.1:n.1696C>T
ENST00000682676.1:n.799C>T
ENST00000682902.1:n.1700C>T
ENST00000683513.1:c.1398C>T	ENSP00000506809.1:p.Ile466=
ENST00000263431.4:c.1398C>T MANE Select	ENSP00000263431.3:p.Ile466=
ENST00000263431.3:c.1398C>T	ENSP00000263431.3:p.Ile466=
NM_001316329.1:c.1398C>T	NP_001303258.1:p.Ile466=
NM_002739.3:c.1398C>T , LRG_669t1:c.1398C>T	NP_002730.1:p.Ile466=
NM_002739.4:c.1398C>T	NP_002730.1:p.Ile466=
XM_011527108.1:c.489C>T	XP_011525410.1:p.Ile163=
NM_002739.5:c.1398C>T MANE Select	NP_002730.1:p.Ile466=
NM_001316329.2:c.1398C>T	NP_001303258.1:p.Ile466=