Canonical Allele Identifier: CA391622155

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634267C>T (hg19) ; chr15:g.34342066C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342066C>T , CM000677.2:g.34342066C>T	GRCh38
NC_000015.9:g.34634267C>T , CM000677.1:g.34634267C>T	GRCh37
NC_000015.8:g.32421559C>T	NCBI36
NG_007951.1:g.999G>A , LRG_270:g.999G>A
NG_011562.1:g.6096G>A , LRG_345:g.6096G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-16G>A	ENSP00000453475.1:n.55-16G>A
ENST00000699926.1:c.100G>A	ENSP00000514692.1:p.Ala34Thr
ENST00000699934.1:c.97G>A	ENSP00000514697.1:p.Ala33Thr
ENST00000699935.1:c.121G>A	ENSP00000514698.1:p.Ala41Thr
ENST00000699936.1:c.31G>A	ENSP00000514699.1:p.Ala11Thr
ENST00000699937.1:c.82G>A	ENSP00000514700.1:p.Ala28Thr
ENST00000699938.1:c.97G>A	ENSP00000514701.1:p.Ala33Thr
ENST00000699939.1:n.260-16G>A
ENST00000328848.6:c.97G>A MANE Select	ENSP00000332198.5:p.Ala33Thr
ENST00000328848.5:c.97G>A	ENSP00000332198.4:p.Ala33Thr
ENST00000557912.1:c.55-16G>A	ENSP00000453475.1:n.55-16G>A
NM_018648.3:c.97G>A , LRG_345t1:c.97G>A	NP_061118.1:p.Ala33Thr
NM_018648.4:c.97G>A MANE Select	NP_061118.1:p.Ala33Thr