Canonical Allele Identifier: CA928353708

Gene: PRKG1

Linked Data

• gnomAD v3: 10-51482943-C-CCATTTTAATGTCTTCCTGTTCCAGGAT
• gnomAD v4: 10-51482943-C-CCATTTTAATGTCTTCCTGTTCCAGGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.51482943_51482944insCATTTTAATGTCTTCCTGTTCCAGGAT , CM000672.2:g.51482943_51482944insCATTTTAATGTCTTCCTGTTCCAGGAT	GRCh38
NC_000010.10:g.53242703_53242704insCATTTTAATGTCTTCCTGTTCCAGGAT , CM000672.1:g.53242703_53242704insCATTTTAATGTCTTCCTGTTCCAGGAT	GRCh37
NC_000010.9:g.52912709_52912710insCATTTTAATGTCTTCCTGTTCCAGGAT	NCBI36
NG_029982.1:g.496793_496794insCATTTTAATGTCTTCCTGTTCCAGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373976.9:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000363087.4:n.592+15107_592+15108insCATTTTAATGTCTTCCTGT...
ENST00000373980.11:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT MANE Select	ENSP00000363092.5:n.592+15107_592+15108insCATTTTAATGTCTTCCTGT...
ENST00000401604.8:c.547+15107_547+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000384200.4:n.547+15107_547+15108insCATTTTAATGTCTTCCTGT...
ENST00000643582.1:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000495279.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGT...
ENST00000643704.1:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000496551.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGT...
ENST00000645324.1:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000494124.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGT...
ENST00000645790.1:n.114+15107_114+15108insCATTTTAATGTCTTCCTGTTCCAGGAT
ENST00000373976.8:c.166+15107_166+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000363087.3:n.166+15107_166+15108insCATTTTAATGTCTTCCTGT...
ENST00000373980.8:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000363092.4:n.592+15107_592+15108insCATTTTAATGTCTTCCTGT...
ENST00000373985.5:c.547+15107_547+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	ENSP00000363097.2:n.547+15107_547+15108insCATTTTAATGTCTTCCTGT...
NM_001098512.2:c.547+15107_547+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	NP_001091982.1:n.547+15107_547+15108insCATTTTAATGTCTTCCTGTTCC...
NM_006258.3:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	NP_006249.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGG...
XM_011539952.1:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	XP_011538254.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCC...
NM_001098512.3:c.547+15107_547+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	NP_001091982.1:n.547+15107_547+15108insCATTTTAATGTCTTCCTGTTCC...
NM_006258.4:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT MANE Select	NP_006249.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGG...
XM_011539952.2:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	XP_011538254.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCC...
XM_017016412.1:c.307+15107_307+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	XP_016871901.1:n.307+15107_307+15108insCATTTTAATGTCTTCCTGTTCC...
XM_017016413.1:c.289+15107_289+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	XP_016871902.1:n.289+15107_289+15108insCATTTTAATGTCTTCCTGTTCC...
NM_001374782.1:c.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCCAGGAT	NP_001361711.1:n.592+15107_592+15108insCATTTTAATGTCTTCCTGTTCC...