Canonical Allele Identifier: CA2295008727

Gene: NOL4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.34065415G>C , CM000680.2:g.34065415G>C	GRCh38
NC_000018.9:g.31645379G>C , CM000680.1:g.31645379G>C	GRCh37
NC_000018.8:g.29899377G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261592.10:c.772+28050C>G MANE Select	ENSP00000261592.4:n.772+28050C>G
ENST00000261592.9:c.772+28050C>G	ENSP00000261592.4:n.772+28050C>G
ENST00000538587.5:c.550+28050C>G	ENSP00000443472.1:n.550+28050C>G
ENST00000586314.5:c.*381+28050C>G	ENSP00000464704.1:n.*381+28050C>G
ENST00000589544.5:c.772+28050C>G	ENSP00000465450.1:n.772+28050C>G
ENST00000590712.5:c.724+28050C>G	ENSP00000467629.1:n.724+28050C>G
NM_001198546.1:c.772+28050C>G	NP_001185475.1:n.772+28050C>G
NM_001198547.1:c.550+28050C>G	NP_001185476.1:n.550+28050C>G
NM_001198548.1:c.772+28050C>G	NP_001185477.1:n.772+28050C>G
NM_001282527.1:c.307+28050C>G	NP_001269456.1:n.307+28050C>G
NM_003787.4:c.772+28050C>G	NP_003778.2:n.772+28050C>G
XM_006722563.2:c.772+28050C>G	XP_006722626.1:n.772+28050C>G
XM_006722564.1:c.550+28050C>G	XP_006722627.1:n.550+28050C>G
XM_006722565.1:c.307+28050C>G	XP_006722628.1:n.307+28050C>G
XM_011526237.1:c.772+28050C>G	XP_011524539.1:n.772+28050C>G
XM_011526238.1:c.430+28050C>G	XP_011524540.1:n.430+28050C>G
XM_011526239.1:c.307+28050C>G	XP_011524541.1:n.307+28050C>G
XM_011526240.1:c.307+28050C>G	XP_011524542.1:n.307+28050C>G
XM_011526241.1:c.772+28050C>G	XP_011524543.1:n.772+28050C>G
XR_935261.1:n.1792+28050C>G
NM_001353232.1:c.772+28050C>G	NP_001340161.1:n.772+28050C>G
NM_001353233.1:c.-194+28050C>G	NP_001340162.1:n.-194+28050C>G
NM_001353234.1:c.550+28050C>G	NP_001340163.1:n.550+28050C>G
NM_001353235.1:c.307+28050C>G	NP_001340164.1:n.307+28050C>G
NM_001353237.1:c.307+28050C>G	NP_001340166.1:n.307+28050C>G
XM_006722563.3:c.772+28050C>G	XP_006722626.1:n.772+28050C>G
XM_011526237.2:c.772+28050C>G	XP_011524539.1:n.772+28050C>G
XM_011526238.2:c.430+28050C>G	XP_011524540.1:n.430+28050C>G
XM_011526239.3:c.307+28050C>G	XP_011524541.1:n.307+28050C>G
XM_017026052.2:c.412+28050C>G	XP_016881541.1:n.412+28050C>G
XM_017026053.2:c.307+28050C>G	XP_016881542.1:n.307+28050C>G
XM_017026054.2:c.307+28050C>G	XP_016881543.1:n.307+28050C>G
XM_017026055.2:c.307+28050C>G	XP_016881544.1:n.307+28050C>G
XM_017026058.2:c.307+28050C>G	XP_016881547.1:n.307+28050C>G
XM_017026059.2:c.-148-6497C>G	XP_016881548.1:n.-148-6497C>G
XM_024451279.1:c.430+28050C>G	XP_024307047.1:n.430+28050C>G
XR_002958188.1:n.945-6497C>G
XR_935261.3:n.944+28050C>G
NM_001198547.2:c.550+28050C>G	NP_001185476.1:n.550+28050C>G
NM_001282527.2:c.307+28050C>G	NP_001269456.1:n.307+28050C>G
NM_001353234.2:c.550+28050C>G	NP_001340163.1:n.550+28050C>G
NM_001353235.2:c.307+28050C>G	NP_001340164.1:n.307+28050C>G
NM_001384467.1:c.841+28050C>G	NP_001371396.1:n.841+28050C>G
NM_001384468.1:c.841+28050C>G	NP_001371397.1:n.841+28050C>G
NM_001384469.1:c.835+28050C>G	NP_001371398.1:n.835+28050C>G
NM_001384470.1:c.430+28050C>G	NP_001371399.1:n.430+28050C>G
NM_001384471.1:c.307+28050C>G	NP_001371400.1:n.307+28050C>G
NM_001384472.1:c.-148-6497C>G	NP_001371401.1:n.-148-6497C>G
NM_001384473.1:c.-194+28050C>G	NP_001371402.1:n.-194+28050C>G
NM_003787.5:c.772+28050C>G MANE Select	NP_003778.2:n.772+28050C>G