Canonical Allele Identifier: CA5503738

Gene: PRKG1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52161958A>G , CM000672.2:g.52161958A>G	GRCh38
NC_000010.10:g.53921718A>G , CM000672.1:g.53921718A>G	GRCh37
NC_000010.9:g.53591724A>G	NCBI36
NG_029982.1:g.1175808A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373975.3:n.430A>G
ENST00000373980.11:c.1071A>G MANE Select	ENSP00000363092.5:p.Lys357=
ENST00000401604.8:c.1026A>G	ENSP00000384200.4:p.Lys342=
ENST00000646354.1:n.910A>G
ENST00000672084.1:c.222A>G	ENSP00000499822.1:p.Lys74=
ENST00000373975.2:n.520A>G
ENST00000373980.8:c.1071A>G	ENSP00000363092.4:p.Lys357=
ENST00000373985.5:c.1026A>G	ENSP00000363097.2:p.Lys342=
ENST00000401604.6:c.390A>G	ENSP00000384200.3:p.Lys130=
NM_001098512.2:c.1026A>G	NP_001091982.1:p.Lys342=
NM_006258.3:c.1071A>G	NP_006249.1:p.Lys357=
XM_005269972.3:c.222A>G	XP_005270029.1:p.Lys74=
XM_011539952.1:c.1071A>G	XP_011538254.1:p.Lys357=
NM_001098512.3:c.1026A>G	NP_001091982.1:p.Lys342=
NM_006258.4:c.1071A>G MANE Select	NP_006249.1:p.Lys357=
XM_011539952.2:c.1071A>G	XP_011538254.1:p.Lys357=
XM_017016412.1:c.786A>G	XP_016871901.1:p.Lys262=
XM_017016413.1:c.768A>G	XP_016871902.1:p.Lys256=
XM_024448078.1:c.-139A>G	XP_024303846.1:n.-139A>G
NM_001374781.1:c.-139A>G	NP_001361710.1:n.-139A>G