Canonical Allele Identifier: CA489410072

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634277T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342076T>C , CM000677.2:g.34342076T>C	GRCh38
NC_000015.9:g.34634277T>C , CM000677.1:g.34634277T>C	GRCh37
NC_000015.8:g.32421569T>C	NCBI36
NG_007951.1:g.989A>G , LRG_270:g.989A>G
NG_011562.1:g.6086A>G , LRG_345:g.6086A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-26A>G	ENSP00000453475.1:n.55-26A>G
ENST00000699926.1:c.90A>G	ENSP00000514692.1:p.Ser30=
ENST00000699934.1:c.87A>G	ENSP00000514697.1:p.Ser29=
ENST00000699935.1:c.111A>G	ENSP00000514698.1:p.Ser37=
ENST00000699936.1:c.21A>G	ENSP00000514699.1:p.Ser7=
ENST00000699937.1:c.72A>G	ENSP00000514700.1:p.Ser24=
ENST00000699938.1:c.87A>G	ENSP00000514701.1:p.Ser29=
ENST00000699939.1:n.260-26A>G
ENST00000328848.6:c.87A>G MANE Select	ENSP00000332198.5:p.Ser29=
ENST00000328848.5:c.87A>G	ENSP00000332198.4:p.Ser29=
ENST00000557912.1:c.55-26A>G	ENSP00000453475.1:n.55-26A>G
NM_018648.3:c.87A>G , LRG_345t1:c.87A>G	NP_061118.1:p.Ser29=
NM_018648.4:c.87A>G MANE Select	NP_061118.1:p.Ser29=