Canonical Allele Identifier: CA391622157

Gene: NOP10

Linked Data

• ClinVar Variation Id: 1967479
• ClinVar RCV Id: RCV002722072
• MyVariant Identifiers: chr15:g.34634269G>C (hg19) ; chr15:g.34342068G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342068G>C , CM000677.2:g.34342068G>C	GRCh38
NC_000015.9:g.34634269G>C , CM000677.1:g.34634269G>C	GRCh37
NC_000015.8:g.32421561G>C	NCBI36
NG_007951.1:g.997C>G , LRG_270:g.997C>G
NG_011562.1:g.6094C>G , LRG_345:g.6094C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-18C>G	ENSP00000453475.1:n.55-18C>G
ENST00000699926.1:c.98C>G	ENSP00000514692.1:p.Pro33Arg
ENST00000699934.1:c.95C>G	ENSP00000514697.1:p.Pro32Arg
ENST00000699935.1:c.119C>G	ENSP00000514698.1:p.Pro40Arg
ENST00000699936.1:c.29C>G	ENSP00000514699.1:p.Pro10Arg
ENST00000699937.1:c.80C>G	ENSP00000514700.1:p.Pro27Arg
ENST00000699938.1:c.95C>G	ENSP00000514701.1:p.Pro32Arg
ENST00000699939.1:n.260-18C>G
ENST00000328848.6:c.95C>G MANE Select	ENSP00000332198.5:p.Pro32Arg
ENST00000328848.5:c.95C>G	ENSP00000332198.4:p.Pro32Arg
ENST00000557912.1:c.55-18C>G	ENSP00000453475.1:n.55-18C>G
NM_018648.3:c.95C>G , LRG_345t1:c.95C>G	NP_061118.1:p.Pro32Arg
NM_018648.4:c.95C>G MANE Select	NP_061118.1:p.Pro32Arg