Canonical Allele Identifier: CA391621940

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634183G>T (hg19) ; chr15:g.34341982G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341982G>T , CM000677.2:g.34341982G>T	GRCh38
NC_000015.9:g.34634183G>T , CM000677.1:g.34634183G>T	GRCh37
NC_000015.8:g.32421475G>T	NCBI36
NG_007951.1:g.1083C>A , LRG_270:g.1083C>A
NG_011562.1:g.6180C>A , LRG_345:g.6180C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*12C>A	ENSP00000453475.1:n.*12C>A
ENST00000699926.1:c.184C>A	ENSP00000514692.1:p.Arg62Ser
ENST00000699934.1:c.159+22C>A	ENSP00000514697.1:n.159+22C>A
ENST00000699935.1:c.205C>A	ENSP00000514698.1:p.Arg69Ser
ENST00000699936.1:c.115C>A	ENSP00000514699.1:p.Arg39Ser
ENST00000699937.1:c.166C>A	ENSP00000514700.1:p.Arg56Ser
ENST00000699938.1:c.159+22C>A	ENSP00000514701.1:n.159+22C>A
ENST00000699939.1:n.328C>A
ENST00000328848.6:c.181C>A MANE Select	ENSP00000332198.5:p.Arg61Ser
ENST00000328848.5:c.181C>A	ENSP00000332198.4:p.Arg61Ser
ENST00000557912.1:c.*12C>A	ENSP00000453475.1:n.*12C>A
NM_018648.3:c.181C>A , LRG_345t1:c.181C>A	NP_061118.1:p.Arg61Ser
NM_018648.4:c.181C>A MANE Select	NP_061118.1:p.Arg61Ser