Canonical Allele Identifier: CA489410063

Gene: NOP10

Linked Data

• gnomAD v4: 15-34342070-A-G
• COSMIC: COSM3377535
• MyVariant Identifiers: chr15:g.34634271A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342070A>G , CM000677.2:g.34342070A>G	GRCh38
NC_000015.9:g.34634271A>G , CM000677.1:g.34634271A>G	GRCh37
NC_000015.8:g.32421563A>G	NCBI36
NG_007951.1:g.995T>C , LRG_270:g.995T>C
NG_011562.1:g.6092T>C , LRG_345:g.6092T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-20T>C	ENSP00000453475.1:n.55-20T>C
ENST00000699926.1:c.96T>C	ENSP00000514692.1:p.His32=
ENST00000699934.1:c.93T>C	ENSP00000514697.1:p.His31=
ENST00000699935.1:c.117T>C	ENSP00000514698.1:p.His39=
ENST00000699936.1:c.27T>C	ENSP00000514699.1:p.His9=
ENST00000699937.1:c.78T>C	ENSP00000514700.1:p.His26=
ENST00000699938.1:c.93T>C	ENSP00000514701.1:p.His31=
ENST00000699939.1:n.260-20T>C
ENST00000328848.6:c.93T>C MANE Select	ENSP00000332198.5:p.His31=
ENST00000328848.5:c.93T>C	ENSP00000332198.4:p.His31=
ENST00000557912.1:c.55-20T>C	ENSP00000453475.1:n.55-20T>C
NM_018648.3:c.93T>C , LRG_345t1:c.93T>C	NP_061118.1:p.His31=
NM_018648.4:c.93T>C MANE Select	NP_061118.1:p.His31=