Canonical Allele Identifier: CA1471768063

Gene: PRKG2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.81201575_81201576delinsGC , CM000666.2:g.81201575_81201576delinsGC	GRCh38
NC_000004.11:g.82122729_82122730delinsGC , CM000666.1:g.82122729_82122730delinsGC	GRCh37
NC_000004.10:g.82341753_82341754delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264399.6:c.461+3011_461+3012delinsGC MANE Select	ENSP00000264399.1:n.461+3011_461+3012delinsGC
ENST00000264399.5:c.461+3011_461+3012delinsGC	ENSP00000264399.1:n.461+3011_461+3012delinsGC
ENST00000395578.3:c.461+3011_461+3012delinsGC	ENSP00000378945.1:n.461+3011_461+3012delinsGC
ENST00000628926.1:c.461+3011_461+3012delinsGC	ENSP00000486129.1:n.461+3011_461+3012delinsGC
NM_001282485.1:c.461+3011_461+3012delinsGC	NP_001269414.1:n.461+3011_461+3012delinsGC
NM_006259.2:c.461+3011_461+3012delinsGC	NP_006250.1:n.461+3011_461+3012delinsGC
XM_005263126.2:c.461+3011_461+3012delinsGC	XP_005263183.1:n.461+3011_461+3012delinsGC
XM_011532114.1:c.461+3011_461+3012delinsGC	XP_011530416.1:n.461+3011_461+3012delinsGC
XM_011532115.1:c.461+3011_461+3012delinsGC	XP_011530417.1:n.461+3011_461+3012delinsGC
XM_011532116.1:c.461+3011_461+3012delinsGC	XP_011530418.1:n.461+3011_461+3012delinsGC
NM_001363401.1:c.461+3011_461+3012delinsGC	NP_001350330.1:n.461+3011_461+3012delinsGC
XM_017008413.1:c.461+3011_461+3012delinsGC	XP_016863902.1:n.461+3011_461+3012delinsGC
XM_017008414.1:c.461+3011_461+3012delinsGC	XP_016863903.1:n.461+3011_461+3012delinsGC
XM_017008415.1:c.461+3011_461+3012delinsGC	XP_016863904.1:n.461+3011_461+3012delinsGC
XM_017008416.1:c.461+3011_461+3012delinsGC	XP_016863905.1:n.461+3011_461+3012delinsGC
XM_017008417.1:c.461+3011_461+3012delinsGC	XP_016863906.1:n.461+3011_461+3012delinsGC
XM_017008418.1:c.461+3011_461+3012delinsGC	XP_016863907.1:n.461+3011_461+3012delinsGC
NM_001282485.2:c.461+3011_461+3012delinsGC	NP_001269414.1:n.461+3011_461+3012delinsGC
NM_001363401.2:c.461+3011_461+3012delinsGC	NP_001350330.1:n.461+3011_461+3012delinsGC
NM_006259.3:c.461+3011_461+3012delinsGC MANE Select	NP_006250.1:n.461+3011_461+3012delinsGC