Canonical Allele Identifier: CA391622150

Gene: NOP10

Linked Data

• dbSNP Id: rs1382116882
• gnomAD v4: 15-34342065-G-A
• MyVariant Identifiers: chr15:g.34634266G>A (hg19) ; chr15:g.34342065G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342065G>A , CM000677.2:g.34342065G>A	GRCh38
NC_000015.9:g.34634266G>A , CM000677.1:g.34634266G>A	GRCh37
NC_000015.8:g.32421558G>A	NCBI36
NG_007951.1:g.1000C>T , LRG_270:g.1000C>T
NG_011562.1:g.6097C>T , LRG_345:g.6097C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-15C>T	ENSP00000453475.1:n.55-15C>T
ENST00000699926.1:c.101C>T	ENSP00000514692.1:p.Ala34Val
ENST00000699934.1:c.98C>T	ENSP00000514697.1:p.Ala33Val
ENST00000699935.1:c.122C>T	ENSP00000514698.1:p.Ala41Val
ENST00000699936.1:c.32C>T	ENSP00000514699.1:p.Ala11Val
ENST00000699937.1:c.83C>T	ENSP00000514700.1:p.Ala28Val
ENST00000699938.1:c.98C>T	ENSP00000514701.1:p.Ala33Val
ENST00000699939.1:n.260-15C>T
ENST00000328848.6:c.98C>T MANE Select	ENSP00000332198.5:p.Ala33Val
ENST00000328848.5:c.98C>T	ENSP00000332198.4:p.Ala33Val
ENST00000557912.1:c.55-15C>T	ENSP00000453475.1:n.55-15C>T
NM_018648.3:c.98C>T , LRG_345t1:c.98C>T	NP_061118.1:p.Ala33Val
NM_018648.4:c.98C>T MANE Select	NP_061118.1:p.Ala33Val