Canonical Allele Identifier: CA2838491035

Gene: PRKG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.51962929A>G , CM000672.2:g.51962929A>G	GRCh38
NC_000010.10:g.53722689A>G , CM000672.1:g.53722689A>G	GRCh37
NC_000010.9:g.53392695A>G	NCBI36
NG_029982.1:g.976779A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373976.9:c.762+55359A>G	ENSP00000363087.4:n.762+55359A>G
ENST00000373980.11:c.762+55359A>G MANE Select	ENSP00000363092.5:n.762+55359A>G
ENST00000401604.8:c.717+55359A>G	ENSP00000384200.4:n.717+55359A>G
ENST00000645324.1:c.762+55359A>G	ENSP00000494124.1:n.762+55359A>G
ENST00000373976.8:c.336+55359A>G	ENSP00000363087.3:n.336+55359A>G
ENST00000373980.8:c.762+55359A>G	ENSP00000363092.4:n.762+55359A>G
ENST00000373985.5:c.717+55359A>G	ENSP00000363097.2:n.717+55359A>G
ENST00000401604.6:c.81+55359A>G	ENSP00000384200.3:n.81+55359A>G
NM_001098512.2:c.717+55359A>G	NP_001091982.1:n.717+55359A>G
NM_006258.3:c.762+55359A>G	NP_006249.1:n.762+55359A>G
XM_011539952.1:c.762+55359A>G	XP_011538254.1:n.762+55359A>G
NM_001098512.3:c.717+55359A>G	NP_001091982.1:n.717+55359A>G
NM_006258.4:c.762+55359A>G MANE Select	NP_006249.1:n.762+55359A>G
XM_011539952.2:c.762+55359A>G	XP_011538254.1:n.762+55359A>G
XM_017016412.1:c.477+55359A>G	XP_016871901.1:n.477+55359A>G
XM_017016413.1:c.459+55359A>G	XP_016871902.1:n.459+55359A>G
NM_001374782.1:c.762+55359A>G	NP_001361711.1:n.762+55359A>G