Canonical Allele Identifier: CA489409942

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634184C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341983C>G , CM000677.2:g.34341983C>G	GRCh38
NC_000015.9:g.34634184C>G , CM000677.1:g.34634184C>G	GRCh37
NC_000015.8:g.32421476C>G	NCBI36
NG_007951.1:g.1082G>C , LRG_270:g.1082G>C
NG_011562.1:g.6179G>C , LRG_345:g.6179G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*11G>C	ENSP00000453475.1:n.*11G>C
ENST00000699926.1:c.183G>C	ENSP00000514692.1:p.Pro61=
ENST00000699934.1:c.159+21G>C	ENSP00000514697.1:n.159+21G>C
ENST00000699935.1:c.204G>C	ENSP00000514698.1:p.Pro68=
ENST00000699936.1:c.114G>C	ENSP00000514699.1:p.Pro38=
ENST00000699937.1:c.165G>C	ENSP00000514700.1:p.Pro55=
ENST00000699938.1:c.159+21G>C	ENSP00000514701.1:n.159+21G>C
ENST00000699939.1:n.327G>C
ENST00000328848.6:c.180G>C MANE Select	ENSP00000332198.5:p.Pro60=
ENST00000328848.5:c.180G>C	ENSP00000332198.4:p.Pro60=
ENST00000557912.1:c.*11G>C	ENSP00000453475.1:n.*11G>C
NM_018648.3:c.180G>C , LRG_345t1:c.180G>C	NP_061118.1:p.Pro60=
NM_018648.4:c.180G>C MANE Select	NP_061118.1:p.Pro60=