Canonical Allele Identifier: CA391622336

Gene: NOP10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34343043C>G , CM000677.2:g.34343043C>G	GRCh38
NC_000015.9:g.34635244C>G , CM000677.1:g.34635244C>G	GRCh37
NC_000015.8:g.32422536C>G	NCBI36
NG_007951.1:g.22G>C , LRG_270:g.22G>C
NG_011562.1:g.5119G>C , LRG_345:g.5119G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018648.4:c.31G>C MANE Select	NP_061118.1:p.Gly11Arg
ENST00000328848.6:c.31G>C MANE Select	ENSP00000332198.5:p.Gly11Arg
NM_018648.3:c.31G>C , LRG_345t1:c.31G>C	NP_061118.1:p.Gly11Arg
ENST00000328848.5:c.31G>C	ENSP00000332198.4:p.Gly11Arg
ENST00000557912.1:c.31G>C	ENSP00000453475.1:p.Gly11Arg
ENST00000557912.2:c.31G>C	ENSP00000453475.1:p.Gly11Arg
ENST00000699926.1:c.31G>C	ENSP00000514692.1:p.Gly11Arg
ENST00000699934.1:c.31G>C	ENSP00000514697.1:p.Gly11Arg
ENST00000699935.1:c.-289G>C	ENSP00000514698.1:n.-289G>C
ENST00000699936.1:c.-155G>C	ENSP00000514699.1:n.-155G>C
ENST00000699937.1:c.31G>C	ENSP00000514700.1:p.Gly11Arg
ENST00000699938.1:c.31G>C	ENSP00000514701.1:p.Gly11Arg
ENST00000699939.1:n.117G>C