Canonical Allele Identifier: CA928339588

Gene: PRKG1

Linked Data

• dbSNP Id: rs1841073072
• gnomAD v3: 10-51502895-G-A
• gnomAD v4: 10-51502895-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.51502895G>A , CM000672.2:g.51502895G>A	GRCh38
NC_000010.10:g.53262655G>A , CM000672.1:g.53262655G>A	GRCh37
NC_000010.9:g.52932661G>A	NCBI36
NG_029982.1:g.516745G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373976.9:c.592+35059G>A	ENSP00000363087.4:n.592+35059G>A
ENST00000373980.11:c.592+35059G>A MANE Select	ENSP00000363092.5:n.592+35059G>A
ENST00000401604.8:c.547+35059G>A	ENSP00000384200.4:n.547+35059G>A
ENST00000643582.1:c.592+35059G>A	ENSP00000495279.1:n.592+35059G>A
ENST00000643704.1:c.592+35059G>A	ENSP00000496551.1:n.592+35059G>A
ENST00000645324.1:c.592+35059G>A	ENSP00000494124.1:n.592+35059G>A
ENST00000645790.1:n.114+35059G>A
ENST00000373976.8:c.166+35059G>A	ENSP00000363087.3:n.166+35059G>A
ENST00000373980.8:c.592+35059G>A	ENSP00000363092.4:n.592+35059G>A
ENST00000373985.5:c.547+35059G>A	ENSP00000363097.2:n.547+35059G>A
NM_001098512.2:c.547+35059G>A	NP_001091982.1:n.547+35059G>A
NM_006258.3:c.592+35059G>A	NP_006249.1:n.592+35059G>A
XM_011539952.1:c.592+35059G>A	XP_011538254.1:n.592+35059G>A
NM_001098512.3:c.547+35059G>A	NP_001091982.1:n.547+35059G>A
NM_006258.4:c.592+35059G>A MANE Select	NP_006249.1:n.592+35059G>A
XM_011539952.2:c.592+35059G>A	XP_011538254.1:n.592+35059G>A
XM_017016412.1:c.307+35059G>A	XP_016871901.1:n.307+35059G>A
XM_017016413.1:c.289+35059G>A	XP_016871902.1:n.289+35059G>A
NM_001374782.1:c.592+35059G>A	NP_001361711.1:n.592+35059G>A