Canonical Allele Identifier: CA2627640071

Gene: NOP10

Linked Data

• gnomAD v4: 15-34341866-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341866T>C , CM000677.2:g.34341866T>C	GRCh38
NC_000015.9:g.34634067T>C , CM000677.1:g.34634067T>C	GRCh37
NC_000015.8:g.32421359T>C	NCBI36
NG_007951.1:g.1199A>G , LRG_270:g.1199A>G
NG_011562.1:g.6296A>G , LRG_345:g.6296A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.*128A>G	ENSP00000453475.1:n.*128A>G
ENST00000699926.1:c.*102A>G	ENSP00000514692.1:n.*102A>G
ENST00000699934.1:c.159+138A>G	ENSP00000514697.1:n.159+138A>G
ENST00000699935.1:c.*102A>G	ENSP00000514698.1:n.*102A>G
ENST00000699936.1:c.*102A>G	ENSP00000514699.1:n.*102A>G
ENST00000699937.1:c.*102A>G	ENSP00000514700.1:n.*102A>G
ENST00000699938.1:c.*46A>G	ENSP00000514701.1:n.*46A>G
ENST00000699939.1:n.444A>G
ENST00000328848.6:c.*102A>G MANE Select	ENSP00000332198.5:n.*102A>G
ENST00000328848.5:c.*102A>G	ENSP00000332198.4:n.*102A>G
ENST00000557912.1:c.*128A>G	ENSP00000453475.1:n.*128A>G
NM_018648.3:c.*102A>G , LRG_345t1:c.*102A>G	NP_061118.1:n.*102A>G
NM_018648.4:c.*102A>G MANE Select	NP_061118.1:n.*102A>G