Canonical Allele Identifier: CA928353669

Gene: PRKG1

Linked Data

• dbSNP Id: rs1840405574
• gnomAD v3: 10-51482862-A-G
• gnomAD v4: 10-51482862-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.51482862A>G , CM000672.2:g.51482862A>G	GRCh38
NC_000010.10:g.53242622A>G , CM000672.1:g.53242622A>G	GRCh37
NC_000010.9:g.52912628A>G	NCBI36
NG_029982.1:g.496712A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373976.9:c.592+15026A>G	ENSP00000363087.4:n.592+15026A>G
ENST00000373980.11:c.592+15026A>G MANE Select	ENSP00000363092.5:n.592+15026A>G
ENST00000401604.8:c.547+15026A>G	ENSP00000384200.4:n.547+15026A>G
ENST00000643582.1:c.592+15026A>G	ENSP00000495279.1:n.592+15026A>G
ENST00000643704.1:c.592+15026A>G	ENSP00000496551.1:n.592+15026A>G
ENST00000645324.1:c.592+15026A>G	ENSP00000494124.1:n.592+15026A>G
ENST00000645790.1:n.114+15026A>G
ENST00000373976.8:c.166+15026A>G	ENSP00000363087.3:n.166+15026A>G
ENST00000373980.8:c.592+15026A>G	ENSP00000363092.4:n.592+15026A>G
ENST00000373985.5:c.547+15026A>G	ENSP00000363097.2:n.547+15026A>G
NM_001098512.2:c.547+15026A>G	NP_001091982.1:n.547+15026A>G
NM_006258.3:c.592+15026A>G	NP_006249.1:n.592+15026A>G
XM_011539952.1:c.592+15026A>G	XP_011538254.1:n.592+15026A>G
NM_001098512.3:c.547+15026A>G	NP_001091982.1:n.547+15026A>G
NM_006258.4:c.592+15026A>G MANE Select	NP_006249.1:n.592+15026A>G
XM_011539952.2:c.592+15026A>G	XP_011538254.1:n.592+15026A>G
XM_017016412.1:c.307+15026A>G	XP_016871901.1:n.307+15026A>G
XM_017016413.1:c.289+15026A>G	XP_016871902.1:n.289+15026A>G
NM_001374782.1:c.592+15026A>G	NP_001361711.1:n.592+15026A>G