Canonical Allele Identifier: CA391622108

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634247G>C (hg19) ; chr15:g.34342046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342046G>C , CM000677.2:g.34342046G>C	GRCh38
NC_000015.9:g.34634247G>C , CM000677.1:g.34634247G>C	GRCh37
NC_000015.8:g.32421539G>C	NCBI36
NG_007951.1:g.1019C>G , LRG_270:g.1019C>G
NG_011562.1:g.6116C>G , LRG_345:g.6116C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.59C>G	ENSP00000453475.1:p.Thr20Arg
ENST00000699926.1:c.120C>G	ENSP00000514692.1:p.Asp40Glu
ENST00000699934.1:c.117C>G	ENSP00000514697.1:p.Asp39Glu
ENST00000699935.1:c.141C>G	ENSP00000514698.1:p.Asp47Glu
ENST00000699936.1:c.51C>G	ENSP00000514699.1:p.Asp17Glu
ENST00000699937.1:c.102C>G	ENSP00000514700.1:p.Asp34Glu
ENST00000699938.1:c.117C>G	ENSP00000514701.1:p.Asp39Glu
ENST00000699939.1:n.264C>G
ENST00000328848.6:c.117C>G MANE Select	ENSP00000332198.5:p.Asp39Glu
ENST00000328848.5:c.117C>G	ENSP00000332198.4:p.Asp39Glu
ENST00000557912.1:c.59C>G	ENSP00000453475.1:p.Thr20Arg
NM_018648.3:c.117C>G , LRG_345t1:c.117C>G	NP_061118.1:p.Asp39Glu
NM_018648.4:c.117C>G MANE Select	NP_061118.1:p.Asp39Glu