Canonical Allele Identifier: CA2842061055

Gene: NOP10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341875C>T , CM000677.2:g.34341875C>T	GRCh38
NC_000015.9:g.34634076C>T , CM000677.1:g.34634076C>T	GRCh37
NC_000015.8:g.32421368C>T	NCBI36
NG_007951.1:g.1190G>A , LRG_270:g.1190G>A
NG_011562.1:g.6287G>A , LRG_345:g.6287G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.*119G>A	ENSP00000453475.1:n.*119G>A
ENST00000699926.1:c.*93G>A	ENSP00000514692.1:n.*93G>A
ENST00000699934.1:c.159+129G>A	ENSP00000514697.1:n.159+129G>A
ENST00000699935.1:c.*93G>A	ENSP00000514698.1:n.*93G>A
ENST00000699936.1:c.*93G>A	ENSP00000514699.1:n.*93G>A
ENST00000699937.1:c.*93G>A	ENSP00000514700.1:n.*93G>A
ENST00000699938.1:c.*37G>A	ENSP00000514701.1:n.*37G>A
ENST00000699939.1:n.435G>A
ENST00000328848.6:c.*93G>A MANE Select	ENSP00000332198.5:n.*93G>A
ENST00000328848.5:c.*93G>A	ENSP00000332198.4:n.*93G>A
ENST00000557912.1:c.*119G>A	ENSP00000453475.1:n.*119G>A
NM_018648.3:c.*93G>A , LRG_345t1:c.*93G>A	NP_061118.1:n.*93G>A
NM_018648.4:c.*93G>A MANE Select	NP_061118.1:n.*93G>A