Canonical Allele Identifier: CA7464779

Gene: NOP10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342088T>A , CM000677.2:g.34342088T>A	GRCh38
NC_000015.9:g.34634289T>A , CM000677.1:g.34634289T>A	GRCh37
NC_000015.8:g.32421581T>A	NCBI36
NG_007951.1:g.977A>T , LRG_270:g.977A>T
NG_011562.1:g.6074A>T , LRG_345:g.6074A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018648.4:c.75A>T MANE Select	NP_061118.1:p.Gln25His
ENST00000328848.6:c.75A>T MANE Select	ENSP00000332198.5:p.Gln25His
NM_018648.3:c.75A>T , LRG_345t1:c.75A>T	NP_061118.1:p.Gln25His
ENST00000328848.5:c.75A>T	ENSP00000332198.4:p.Gln25His
ENST00000557912.1:c.55-38A>T	ENSP00000453475.1:n.55-38A>T
ENST00000557912.2:c.55-38A>T	ENSP00000453475.1:n.55-38A>T
ENST00000699926.1:c.78A>T	ENSP00000514692.1:p.Gln26His
ENST00000699934.1:c.75A>T	ENSP00000514697.1:p.Gln25His
ENST00000699935.1:c.99A>T	ENSP00000514698.1:p.Gln33His
ENST00000699936.1:c.9A>T	ENSP00000514699.1:p.Gln3His
ENST00000699937.1:c.60A>T	ENSP00000514700.1:p.Gln20His
ENST00000699938.1:c.75A>T	ENSP00000514701.1:p.Gln25His
ENST00000699939.1:n.260-38A>T