Canonical Allele Identifier: CA997084061
Gene: PRKCG HGNC NCBI

Linked Data

dbSNP Id: rs2068755898
gnomAD v3: 19-53900549-G-A
gnomAD v4: 19-53900549-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900549G>A , CM000681.2:g.53900549G>A GRCh38
NC_000019.9:g.54403803G>A , CM000681.1:g.54403803G>A GRCh37
NC_000019.8:g.59095615G>A NCBI36
NG_009114.1:g.23337G>A , LRG_669:g.23337G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.1437-62G>A ENSP00000507230.1:n.1437-62G>A
ENST00000682268.1:n.1735-62G>A
ENST00000682676.1:n.838-62G>A
ENST00000682902.1:n.1739-62G>A
ENST00000683513.1:c.1437-62G>A ENSP00000506809.1:n.1437-62G>A
ENST00000263431.4:c.1437-62G>A MANE Select ENSP00000263431.3:n.1437-62G>A
ENST00000263431.3:c.1437-62G>A ENSP00000263431.3:n.1437-62G>A
NM_001316329.1:c.1437-62G>A NP_001303258.1:n.1437-62G>A
NM_002739.3:c.1437-62G>A , LRG_669t1:c.1437-62G>A NP_002730.1:n.1437-62G>A
NM_002739.4:c.1437-62G>A NP_002730.1:n.1437-62G>A
XM_011527108.1:c.528-62G>A XP_011525410.1:n.528-62G>A
NM_002739.5:c.1437-62G>A MANE Select NP_002730.1:n.1437-62G>A
NM_001316329.2:c.1437-62G>A NP_001303258.1:n.1437-62G>A
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