Canonical Allele Identifier: CA666235897
Gene: PRKG1 HGNC NCBI

Linked Data

dbSNP Id: rs1237953708

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.51482925T>C , CM000672.2:g.51482925T>C GRCh38
NC_000010.10:g.53242685T>C , CM000672.1:g.53242685T>C GRCh37
NC_000010.9:g.52912691T>C NCBI36
NG_029982.1:g.496775T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373976.9:c.592+15089T>C ENSP00000363087.4:n.592+15089T>C
ENST00000373980.11:c.592+15089T>C MANE Select ENSP00000363092.5:n.592+15089T>C
ENST00000401604.8:c.547+15089T>C ENSP00000384200.4:n.547+15089T>C
ENST00000643582.1:c.592+15089T>C ENSP00000495279.1:n.592+15089T>C
ENST00000643704.1:c.592+15089T>C ENSP00000496551.1:n.592+15089T>C
ENST00000645324.1:c.592+15089T>C ENSP00000494124.1:n.592+15089T>C
ENST00000645790.1:n.114+15089T>C
ENST00000373976.8:c.166+15089T>C ENSP00000363087.3:n.166+15089T>C
ENST00000373980.8:c.592+15089T>C ENSP00000363092.4:n.592+15089T>C
ENST00000373985.5:c.547+15089T>C ENSP00000363097.2:n.547+15089T>C
NM_001098512.2:c.547+15089T>C NP_001091982.1:n.547+15089T>C
NM_006258.3:c.592+15089T>C NP_006249.1:n.592+15089T>C
XM_011539952.1:c.592+15089T>C XP_011538254.1:n.592+15089T>C
NM_001098512.3:c.547+15089T>C NP_001091982.1:n.547+15089T>C
NM_006258.4:c.592+15089T>C MANE Select NP_006249.1:n.592+15089T>C
XM_011539952.2:c.592+15089T>C XP_011538254.1:n.592+15089T>C
XM_017016412.1:c.307+15089T>C XP_016871901.1:n.307+15089T>C
XM_017016413.1:c.289+15089T>C XP_016871902.1:n.289+15089T>C
NM_001374782.1:c.592+15089T>C NP_001361711.1:n.592+15089T>C