Canonical Allele Identifier: CA1909674879
Gene: PRKG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.51502899T= , CM000672.2:g.51502899T= GRCh38
NC_000010.10:g.53262659T= , CM000672.1:g.53262659T= GRCh37
NC_000010.9:g.52932665T= NCBI36
NG_029982.1:g.516749T=

Transcript Alleles

HGVS Amino-acid change
ENST00000373976.9:c.592+35063T= ENSP00000363087.4:n.592+35063T=
ENST00000373980.11:c.592+35063T= MANE Select ENSP00000363092.5:n.592+35063T=
ENST00000401604.8:c.547+35063T= ENSP00000384200.4:n.547+35063T=
ENST00000643582.1:c.592+35063T= ENSP00000495279.1:n.592+35063T=
ENST00000643704.1:c.592+35063T= ENSP00000496551.1:n.592+35063T=
ENST00000645324.1:c.592+35063T= ENSP00000494124.1:n.592+35063T=
ENST00000645790.1:n.114+35063T=
ENST00000373976.8:c.166+35063T= ENSP00000363087.3:n.166+35063T=
ENST00000373980.8:c.592+35063T= ENSP00000363092.4:n.592+35063T=
ENST00000373985.5:c.547+35063T= ENSP00000363097.2:n.547+35063T=
NM_001098512.2:c.547+35063T= NP_001091982.1:n.547+35063T=
NM_006258.3:c.592+35063T= NP_006249.1:n.592+35063T=
XM_011539952.1:c.592+35063T= XP_011538254.1:n.592+35063T=
NM_001098512.3:c.547+35063T= NP_001091982.1:n.547+35063T=
NM_006258.4:c.592+35063T= MANE Select NP_006249.1:n.592+35063T=
XM_011539952.2:c.592+35063T= XP_011538254.1:n.592+35063T=
XM_017016412.1:c.307+35063T= XP_016871901.1:n.307+35063T=
XM_017016413.1:c.289+35063T= XP_016871902.1:n.289+35063T=
NM_001374782.1:c.592+35063T= NP_001361711.1:n.592+35063T=