Canonical Allele Identifier: CA2983906

Gene: PRKG2 PRKG2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.81171781C>G , CM000666.2:g.81171781C>G	GRCh38
NC_000004.11:g.82092935C>G , CM000666.1:g.82092935C>G	GRCh37
NC_000004.10:g.82311959C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006259.3:c.652G>C (PRKG2) MANE Select	NP_006250.1:p.Gly218Arg
ENST00000264399.6:c.652G>C (PRKG2) MANE Select	ENSP00000264399.1:p.Gly218Arg
NM_001282485.1:c.652G>C (PRKG2)	NP_001269414.1:p.Gly218Arg
NM_001282485.2:c.652G>C (PRKG2)	NP_001269414.1:p.Gly218Arg
NM_001363401.1:c.652G>C (PRKG2)	NP_001350330.1:p.Gly218Arg
NM_001363401.2:c.652G>C (PRKG2)	NP_001350330.1:p.Gly218Arg
NM_006259.2:c.652G>C (PRKG2)	NP_006250.1:p.Gly218Arg
NR_125908.1:n.60-1978C>G (PRKG2-AS1)
ENST00000264399.5:c.652G>C (PRKG2)	ENSP00000264399.1:p.Gly218Arg
ENST00000395578.3:c.652G>C (PRKG2)	ENSP00000378945.1:p.Gly218Arg
ENST00000628926.1:c.652G>C (PRKG2)	ENSP00000486129.1:p.Gly218Arg
XM_005263126.2:c.652G>C (PRKG2)	XP_005263183.1:p.Gly218Arg
XM_011532114.1:c.652G>C (PRKG2)	XP_011530416.1:p.Gly218Arg
XM_011532115.1:c.652G>C (PRKG2)	XP_011530417.1:p.Gly218Arg
XM_011532116.1:c.652G>C (PRKG2)	XP_011530418.1:p.Gly218Arg
XM_017008413.1:c.652G>C (PRKG2)	XP_016863902.1:p.Gly218Arg
XM_017008414.1:c.652G>C (PRKG2)	XP_016863903.1:p.Gly218Arg
XM_017008415.1:c.652G>C (PRKG2)	XP_016863904.1:p.Gly218Arg
XM_017008416.1:c.652G>C (PRKG2)	XP_016863905.1:p.Gly218Arg
XM_017008417.1:c.652G>C (PRKG2)	XP_016863906.1:p.Gly218Arg
XM_017008418.1:c.652G>C (PRKG2)	XP_016863907.1:p.Gly218Arg