Canonical Allele Identifier: CA391621926

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634176A>T (hg19) ; chr15:g.34341975A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341975A>T , CM000677.2:g.34341975A>T	GRCh38
NC_000015.9:g.34634176A>T , CM000677.1:g.34634176A>T	GRCh37
NC_000015.8:g.32421468A>T	NCBI36
NG_007951.1:g.1090T>A , LRG_270:g.1090T>A
NG_011562.1:g.6187T>A , LRG_345:g.6187T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*19T>A	ENSP00000453475.1:n.*19T>A
ENST00000699926.1:c.191T>A	ENSP00000514692.1:p.Val64Asp
ENST00000699934.1:c.159+29T>A	ENSP00000514697.1:n.159+29T>A
ENST00000699935.1:c.212T>A	ENSP00000514698.1:p.Val71Asp
ENST00000699936.1:c.122T>A	ENSP00000514699.1:p.Val41Asp
ENST00000699937.1:c.173T>A	ENSP00000514700.1:p.Val58Asp
ENST00000699938.1:c.159+29T>A	ENSP00000514701.1:n.159+29T>A
ENST00000699939.1:n.335T>A
ENST00000328848.6:c.188T>A MANE Select	ENSP00000332198.5:p.Val63Asp
ENST00000328848.5:c.188T>A	ENSP00000332198.4:p.Val63Asp
ENST00000557912.1:c.*19T>A	ENSP00000453475.1:n.*19T>A
NM_018648.3:c.188T>A , LRG_345t1:c.188T>A	NP_061118.1:p.Val63Asp
NM_018648.4:c.188T>A MANE Select	NP_061118.1:p.Val63Asp