Canonical Allele Identifier: CA15652619
Gene: PRKG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.51733713G>A , CM000672.2:g.51733713G>A GRCh38
NC_000010.10:g.53493473G>A , CM000672.1:g.53493473G>A GRCh37
NC_000010.9:g.53163479G>A NCBI36
NG_029982.1:g.747563G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373976.9:c.593-70872G>A ENSP00000363087.4:n.593-70872G>A
ENST00000373980.11:c.593-70872G>A MANE Select ENSP00000363092.5:n.593-70872G>A
ENST00000401604.8:c.548-70872G>A ENSP00000384200.4:n.548-70872G>A
ENST00000643582.1:c.593-70872G>A ENSP00000495279.1:n.593-70872G>A
ENST00000643704.1:c.593-70872G>A ENSP00000496551.1:n.593-70872G>A
ENST00000645324.1:c.593-70872G>A ENSP00000494124.1:n.593-70872G>A
ENST00000373976.8:c.167-70872G>A ENSP00000363087.3:n.167-70872G>A
ENST00000373980.8:c.593-70872G>A ENSP00000363092.4:n.593-70872G>A
ENST00000373985.5:c.548-70872G>A ENSP00000363097.2:n.548-70872G>A
NM_001098512.2:c.548-70872G>A NP_001091982.1:n.548-70872G>A
NM_006258.3:c.593-70872G>A NP_006249.1:n.593-70872G>A
XM_011539952.1:c.593-70872G>A XP_011538254.1:n.593-70872G>A
XR_945960.1:n.174+102C>T
NM_001098512.3:c.548-70872G>A NP_001091982.1:n.548-70872G>A
NM_006258.4:c.593-70872G>A MANE Select NP_006249.1:n.593-70872G>A
XM_011539952.2:c.593-70872G>A XP_011538254.1:n.593-70872G>A
XM_017016412.1:c.308-70872G>A XP_016871901.1:n.308-70872G>A
XM_017016413.1:c.290-70872G>A XP_016871902.1:n.290-70872G>A
NM_001374782.1:c.593-70872G>A NP_001361711.1:n.593-70872G>A