Canonical Allele Identifier: CA391622154

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634267C>G (hg19) ; chr15:g.34342066C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342066C>G , CM000677.2:g.34342066C>G	GRCh38
NC_000015.9:g.34634267C>G , CM000677.1:g.34634267C>G	GRCh37
NC_000015.8:g.32421559C>G	NCBI36
NG_007951.1:g.999G>C , LRG_270:g.999G>C
NG_011562.1:g.6096G>C , LRG_345:g.6096G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-16G>C	ENSP00000453475.1:n.55-16G>C
ENST00000699926.1:c.100G>C	ENSP00000514692.1:p.Ala34Pro
ENST00000699934.1:c.97G>C	ENSP00000514697.1:p.Ala33Pro
ENST00000699935.1:c.121G>C	ENSP00000514698.1:p.Ala41Pro
ENST00000699936.1:c.31G>C	ENSP00000514699.1:p.Ala11Pro
ENST00000699937.1:c.82G>C	ENSP00000514700.1:p.Ala28Pro
ENST00000699938.1:c.97G>C	ENSP00000514701.1:p.Ala33Pro
ENST00000699939.1:n.260-16G>C
ENST00000328848.6:c.97G>C MANE Select	ENSP00000332198.5:p.Ala33Pro
ENST00000328848.5:c.97G>C	ENSP00000332198.4:p.Ala33Pro
ENST00000557912.1:c.55-16G>C	ENSP00000453475.1:n.55-16G>C
NM_018648.3:c.97G>C , LRG_345t1:c.97G>C	NP_061118.1:p.Ala33Pro
NM_018648.4:c.97G>C MANE Select	NP_061118.1:p.Ala33Pro