Canonical Allele Identifier: CA391621929

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634177C>T (hg19) ; chr15:g.34341976C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341976C>T , CM000677.2:g.34341976C>T	GRCh38
NC_000015.9:g.34634177C>T , CM000677.1:g.34634177C>T	GRCh37
NC_000015.8:g.32421469C>T	NCBI36
NG_007951.1:g.1089G>A , LRG_270:g.1089G>A
NG_011562.1:g.6186G>A , LRG_345:g.6186G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*18G>A	ENSP00000453475.1:n.*18G>A
ENST00000699926.1:c.190G>A	ENSP00000514692.1:p.Val64Ile
ENST00000699934.1:c.159+28G>A	ENSP00000514697.1:n.159+28G>A
ENST00000699935.1:c.211G>A	ENSP00000514698.1:p.Val71Ile
ENST00000699936.1:c.121G>A	ENSP00000514699.1:p.Val41Ile
ENST00000699937.1:c.172G>A	ENSP00000514700.1:p.Val58Ile
ENST00000699938.1:c.159+28G>A	ENSP00000514701.1:n.159+28G>A
ENST00000699939.1:n.334G>A
ENST00000328848.6:c.187G>A MANE Select	ENSP00000332198.5:p.Val63Ile
ENST00000328848.5:c.187G>A	ENSP00000332198.4:p.Val63Ile
ENST00000557912.1:c.*18G>A	ENSP00000453475.1:n.*18G>A
NM_018648.3:c.187G>A , LRG_345t1:c.187G>A	NP_061118.1:p.Val63Ile
NM_018648.4:c.187G>A MANE Select	NP_061118.1:p.Val63Ile