Canonical Allele Identifier: CA391622274

Gene: NOP10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34343027G>A , CM000677.2:g.34343027G>A	GRCh38
NC_000015.9:g.34635228G>A , CM000677.1:g.34635228G>A	GRCh37
NC_000015.8:g.32422520G>A	NCBI36
NG_007951.1:g.38C>T , LRG_270:g.38C>T
NG_011562.1:g.5135C>T , LRG_345:g.5135C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018648.4:c.47C>T MANE Select	NP_061118.1:p.Thr16Met
ENST00000328848.6:c.47C>T MANE Select	ENSP00000332198.5:p.Thr16Met
NM_018648.3:c.47C>T , LRG_345t1:c.47C>T	NP_061118.1:p.Thr16Met
ENST00000328848.5:c.47C>T	ENSP00000332198.4:p.Thr16Met
ENST00000557912.1:c.47C>T	ENSP00000453475.1:p.Thr16Met
ENST00000557912.2:c.47C>T	ENSP00000453475.1:p.Thr16Met
ENST00000699926.1:c.47C>T	ENSP00000514692.1:p.Thr16Met
ENST00000699934.1:c.47C>T	ENSP00000514697.1:p.Thr16Met
ENST00000699935.1:c.-273C>T	ENSP00000514698.1:n.-273C>T
ENST00000699936.1:c.-139C>T	ENSP00000514699.1:n.-139C>T
ENST00000699937.1:c.39+8C>T	ENSP00000514700.1:n.39+8C>T
ENST00000699938.1:c.47C>T	ENSP00000514701.1:p.Thr16Met
ENST00000699939.1:n.133C>T