Canonical Allele Identifier: CA391622089

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634240A>G (hg19) ; chr15:g.34342039A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342039A>G , CM000677.2:g.34342039A>G	GRCh38
NC_000015.9:g.34634240A>G , CM000677.1:g.34634240A>G	GRCh37
NC_000015.8:g.32421532A>G	NCBI36
NG_007951.1:g.1026T>C , LRG_270:g.1026T>C
NG_011562.1:g.6123T>C , LRG_345:g.6123T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.66T>C	ENSP00000453475.1:p.Thr22=
ENST00000699926.1:c.127T>C	ENSP00000514692.1:p.Ser43Pro
ENST00000699934.1:c.124T>C	ENSP00000514697.1:p.Ser42Pro
ENST00000699935.1:c.148T>C	ENSP00000514698.1:p.Ser50Pro
ENST00000699936.1:c.58T>C	ENSP00000514699.1:p.Ser20Pro
ENST00000699937.1:c.109T>C	ENSP00000514700.1:p.Ser37Pro
ENST00000699938.1:c.124T>C	ENSP00000514701.1:p.Ser42Pro
ENST00000699939.1:n.271T>C
ENST00000328848.6:c.124T>C MANE Select	ENSP00000332198.5:p.Ser42Pro
ENST00000328848.5:c.124T>C	ENSP00000332198.4:p.Ser42Pro
ENST00000557912.1:c.66T>C	ENSP00000453475.1:p.Thr22=
NM_018648.3:c.124T>C , LRG_345t1:c.124T>C	NP_061118.1:p.Ser42Pro
NM_018648.4:c.124T>C MANE Select	NP_061118.1:p.Ser42Pro