Canonical Allele Identifier: CA407414557

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068660763
• gnomAD v4: 19-53889990-C-T
• MyVariant Identifiers: chr19:g.54393244C>T (hg19) ; chr19:g.53889990C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889990C>T , CM000681.2:g.53889990C>T	GRCh38
NC_000019.9:g.54393244C>T , CM000681.1:g.54393244C>T	GRCh37
NC_000019.8:g.59085056C>T	NCBI36
NG_009114.1:g.12778C>T , LRG_669:g.12778C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.502C>T	ENSP00000507230.1:p.Pro168Ser
ENST00000682268.1:n.800C>T
ENST00000682902.1:n.804C>T
ENST00000683513.1:c.502C>T	ENSP00000506809.1:p.Pro168Ser
ENST00000263431.4:c.502C>T MANE Select	ENSP00000263431.3:p.Pro168Ser
ENST00000263431.3:c.502C>T	ENSP00000263431.3:p.Pro168Ser
ENST00000474397.5:c.118C>T	ENSP00000471271.1:p.Pro40Ser
NM_001316329.1:c.502C>T	NP_001303258.1:p.Pro168Ser
NM_002739.3:c.502C>T , LRG_669t1:c.502C>T	NP_002730.1:p.Pro168Ser
NM_002739.4:c.502C>T	NP_002730.1:p.Pro168Ser
NM_002739.5:c.502C>T MANE Select	NP_002730.1:p.Pro168Ser
NM_001316329.2:c.502C>T	NP_001303258.1:p.Pro168Ser