Canonical Allele Identifier: CA7464777

Gene: NOP10

Linked Data

• dbSNP Id: rs373843596
• ExAC: 15:34634272 T / G
• gnomAD v3: 15-34342071-T-G
• gnomAD v4: 15-34342071-T-G
• MyVariant Identifiers: chr15:g.34634272T>G (hg19) ; chr15:g.34342071T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342071T>G , CM000677.2:g.34342071T>G	GRCh38
NC_000015.9:g.34634272T>G , CM000677.1:g.34634272T>G	GRCh37
NC_000015.8:g.32421564T>G	NCBI36
NG_007951.1:g.994A>C , LRG_270:g.994A>C
NG_011562.1:g.6091A>C , LRG_345:g.6091A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.55-21A>C	ENSP00000453475.1:n.55-21A>C
ENST00000699926.1:c.95A>C	ENSP00000514692.1:p.His32Pro
ENST00000699934.1:c.92A>C	ENSP00000514697.1:p.His31Pro
ENST00000699935.1:c.116A>C	ENSP00000514698.1:p.His39Pro
ENST00000699936.1:c.26A>C	ENSP00000514699.1:p.His9Pro
ENST00000699937.1:c.77A>C	ENSP00000514700.1:p.His26Pro
ENST00000699938.1:c.92A>C	ENSP00000514701.1:p.His31Pro
ENST00000699939.1:n.260-21A>C
ENST00000328848.6:c.92A>C MANE Select	ENSP00000332198.5:p.His31Pro
ENST00000328848.5:c.92A>C	ENSP00000332198.4:p.His31Pro
ENST00000557912.1:c.55-21A>C	ENSP00000453475.1:n.55-21A>C
NM_018648.3:c.92A>C , LRG_345t1:c.92A>C	NP_061118.1:p.His31Pro
NM_018648.4:c.92A>C MANE Select	NP_061118.1:p.His31Pro