Canonical Allele Identifier: CA99631474
Gene: PRKG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.81141777C>T , CM000666.2:g.81141777C>T GRCh38
NC_000004.11:g.82062931C>T , CM000666.1:g.82062931C>T GRCh37
NC_000004.10:g.82281955C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264399.6:c.1407+1017G>A MANE Select ENSP00000264399.1:n.1407+1017G>A
ENST00000264399.5:c.1407+1017G>A ENSP00000264399.1:n.1407+1017G>A
ENST00000395578.3:c.1407+1017G>A ENSP00000378945.1:n.1407+1017G>A
ENST00000456882.2:n.451+1104G>A
ENST00000509169.5:n.677+1017G>A
ENST00000509474.5:n.647+1017G>A
ENST00000545647.5:c.147+1017G>A ENSP00000439967.1:n.147+1017G>A
ENST00000628926.1:c.1320+1104G>A ENSP00000486129.1:n.1320+1104G>A
NM_001282480.1:c.147+1017G>A NP_001269409.1:n.147+1017G>A
NM_001282481.1:c.147+1017G>A NP_001269410.1:n.147+1017G>A
NM_001282482.1:c.60+1104G>A NP_001269411.1:n.60+1104G>A
NM_001282483.1:c.-34+1040G>A NP_001269412.1:n.-34+1040G>A
NM_001282485.1:c.1320+1104G>A NP_001269414.1:n.1320+1104G>A
NM_006259.2:c.1407+1017G>A NP_006250.1:n.1407+1017G>A
XM_005263126.2:c.1407+1017G>A XP_005263183.1:n.1407+1017G>A
XM_006714266.2:c.-34+838G>A XP_006714329.1:n.-34+838G>A
XM_011532114.1:c.1407+1017G>A XP_011530416.1:n.1407+1017G>A
XM_011532115.1:c.1407+1017G>A XP_011530417.1:n.1407+1017G>A
XM_011532116.1:c.1384+1040G>A XP_011530418.1:n.1384+1040G>A
NM_001363401.1:c.1407+1017G>A NP_001350330.1:n.1407+1017G>A
XM_017008413.1:c.1407+1017G>A XP_016863902.1:n.1407+1017G>A
XM_017008414.1:c.1407+1017G>A XP_016863903.1:n.1407+1017G>A
XM_017008415.1:c.1407+1017G>A XP_016863904.1:n.1407+1017G>A
XM_017008416.1:c.1407+1017G>A XP_016863905.1:n.1407+1017G>A
XM_017008417.1:c.1320+1104G>A XP_016863906.1:n.1320+1104G>A
XM_017008418.1:c.1384+1040G>A XP_016863907.1:n.1384+1040G>A
NM_001282485.2:c.1320+1104G>A NP_001269414.1:n.1320+1104G>A
NM_001363401.2:c.1407+1017G>A NP_001350330.1:n.1407+1017G>A
NM_006259.3:c.1407+1017G>A MANE Select NP_006250.1:n.1407+1017G>A
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