Canonical Allele Identifier: CA2576878524

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53890054-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53890054C>T , CM000681.2:g.53890054C>T	GRCh38
NC_000019.9:g.54393308C>T , CM000681.1:g.54393308C>T	GRCh37
NC_000019.8:g.59085120C>T	NCBI36
NG_009114.1:g.12842C>T , LRG_669:g.12842C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.529+37C>T	ENSP00000507230.1:n.529+37C>T
ENST00000682268.1:n.827+37C>T
ENST00000682902.1:n.831+37C>T
ENST00000683513.1:c.529+37C>T	ENSP00000506809.1:n.529+37C>T
ENST00000263431.4:c.529+37C>T MANE Select	ENSP00000263431.3:n.529+37C>T
ENST00000263431.3:c.529+37C>T	ENSP00000263431.3:n.529+37C>T
ENST00000474397.5:c.145+37C>T	ENSP00000471271.1:n.145+37C>T
NM_001316329.1:c.529+37C>T	NP_001303258.1:n.529+37C>T
NM_002739.3:c.529+37C>T , LRG_669t1:c.529+37C>T	NP_002730.1:n.529+37C>T
NM_002739.4:c.529+37C>T	NP_002730.1:n.529+37C>T
NM_002739.5:c.529+37C>T MANE Select	NP_002730.1:n.529+37C>T
NM_001316329.2:c.529+37C>T	NP_001303258.1:n.529+37C>T