Canonical Allele Identifier: CA1471751267

Gene: PRKG2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.81148295G>T , CM000666.2:g.81148295G>T	GRCh38
NC_000004.11:g.82069449G>T , CM000666.1:g.82069449G>T	GRCh37
NC_000004.10:g.82288473G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264399.6:c.1154+589C>A MANE Select	ENSP00000264399.1:n.1154+589C>A
ENST00000264399.5:c.1154+589C>A	ENSP00000264399.1:n.1154+589C>A
ENST00000395578.3:c.1154+589C>A	ENSP00000378945.1:n.1154+589C>A
ENST00000456882.2:n.285+589C>A
ENST00000509169.5:n.424+589C>A
ENST00000509474.5:n.394+589C>A
ENST00000545647.5:c.-107+589C>A	ENSP00000439967.1:n.-107+589C>A
ENST00000628926.1:c.1154+589C>A	ENSP00000486129.1:n.1154+589C>A
NM_001282480.1:c.-107+589C>A	NP_001269409.1:n.-107+589C>A
NM_001282481.1:c.-107+589C>A	NP_001269410.1:n.-107+589C>A
NM_001282482.1:c.-107+589C>A	NP_001269411.1:n.-107+589C>A
NM_001282483.1:c.-264+589C>A	NP_001269412.1:n.-264+589C>A
NM_001282485.1:c.1154+589C>A	NP_001269414.1:n.1154+589C>A
NM_006259.2:c.1154+589C>A	NP_006250.1:n.1154+589C>A
XM_005263126.2:c.1154+589C>A	XP_005263183.1:n.1154+589C>A
XM_011532114.1:c.1154+589C>A	XP_011530416.1:n.1154+589C>A
XM_011532115.1:c.1154+589C>A	XP_011530417.1:n.1154+589C>A
XM_011532116.1:c.1154+589C>A	XP_011530418.1:n.1154+589C>A
NM_001363401.1:c.1154+589C>A	NP_001350330.1:n.1154+589C>A
XM_017008413.1:c.1154+589C>A	XP_016863902.1:n.1154+589C>A
XM_017008414.1:c.1154+589C>A	XP_016863903.1:n.1154+589C>A
XM_017008415.1:c.1154+589C>A	XP_016863904.1:n.1154+589C>A
XM_017008416.1:c.1154+589C>A	XP_016863905.1:n.1154+589C>A
XM_017008417.1:c.1154+589C>A	XP_016863906.1:n.1154+589C>A
XM_017008418.1:c.1154+589C>A	XP_016863907.1:n.1154+589C>A
NM_001282485.2:c.1154+589C>A	NP_001269414.1:n.1154+589C>A
NM_001363401.2:c.1154+589C>A	NP_001350330.1:n.1154+589C>A
NM_006259.3:c.1154+589C>A MANE Select	NP_006250.1:n.1154+589C>A