Canonical Allele Identifier: CA633839354

Gene: PRKCG

Linked Data

• dbSNP Id: rs1309390682
• gnomAD v2: 19-54393265-G-GT
• gnomAD v4: 19-53890011-G-GT
• MyVariant Identifiers: chr19:g.54393265_54393266insT (hg19) ; chr19:g.53890011_53890012insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890012dup , CM000681.2:g.53890012dup	GRCh38
NC_000019.9:g.54393266dup , CM000681.1:g.54393266dup	GRCh37
NC_000019.8:g.59085078dup	NCBI36
NG_009114.1:g.12800dup , LRG_669:g.12800dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.524dup	ENSP00000507230.1:p.Thr176AsnfsTer7
ENST00000682268.1:n.822dup
ENST00000682902.1:n.826dup
ENST00000683513.1:c.524dup	ENSP00000506809.1:p.Thr176AsnfsTer7
ENST00000263431.4:c.524dup MANE Select	ENSP00000263431.3:p.Thr176AsnfsTer7
ENST00000263431.3:c.524dup	ENSP00000263431.3:p.Thr176AsnfsTer7
ENST00000474397.5:c.140dup	ENSP00000471271.1:p.Thr48AsnfsTer7
NM_001316329.1:c.524dup	NP_001303258.1:p.Thr176AsnfsTer7
NM_002739.3:c.524dup , LRG_669t1:c.524dup	NP_002730.1:p.Thr176AsnfsTer7
NM_002739.4:c.524dup	NP_002730.1:p.Thr176AsnfsTer7
NM_002739.5:c.524dup MANE Select	NP_002730.1:p.Thr176AsnfsTer7
NM_001316329.2:c.524dup	NP_001303258.1:p.Thr176AsnfsTer7