Canonical Allele Identifier: CA7464776

Gene: NOP10

Linked Data

• dbSNP Id: rs768707296
• ExAC: 15:34634270 G / C
• gnomAD v2: 15-34634270-G-C
• gnomAD v4: 15-34342069-G-C
• MyVariant Identifiers: chr15:g.34634270G>C (hg19) ; chr15:g.34342069G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342069G>C , CM000677.2:g.34342069G>C	GRCh38
NC_000015.9:g.34634270G>C , CM000677.1:g.34634270G>C	GRCh37
NC_000015.8:g.32421562G>C	NCBI36
NG_007951.1:g.996C>G , LRG_270:g.996C>G
NG_011562.1:g.6093C>G , LRG_345:g.6093C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-19C>G	ENSP00000453475.1:n.55-19C>G
ENST00000699926.1:c.97C>G	ENSP00000514692.1:p.Pro33Ala
ENST00000699934.1:c.94C>G	ENSP00000514697.1:p.Pro32Ala
ENST00000699935.1:c.118C>G	ENSP00000514698.1:p.Pro40Ala
ENST00000699936.1:c.28C>G	ENSP00000514699.1:p.Pro10Ala
ENST00000699937.1:c.79C>G	ENSP00000514700.1:p.Pro27Ala
ENST00000699938.1:c.94C>G	ENSP00000514701.1:p.Pro32Ala
ENST00000699939.1:n.260-19C>G
ENST00000328848.6:c.94C>G MANE Select	ENSP00000332198.5:p.Pro32Ala
ENST00000328848.5:c.94C>G	ENSP00000332198.4:p.Pro32Ala
ENST00000557912.1:c.55-19C>G	ENSP00000453475.1:n.55-19C>G
NM_018648.3:c.94C>G , LRG_345t1:c.94C>G	NP_061118.1:p.Pro32Ala
NM_018648.4:c.94C>G MANE Select	NP_061118.1:p.Pro32Ala