Canonical Allele Identifier: CA391621922

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634174G>C (hg19) ; chr15:g.34341973G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341973G>C , CM000677.2:g.34341973G>C	GRCh38
NC_000015.9:g.34634174G>C , CM000677.1:g.34634174G>C	GRCh37
NC_000015.8:g.32421466G>C	NCBI36
NG_007951.1:g.1092C>G , LRG_270:g.1092C>G
NG_011562.1:g.6189C>G , LRG_345:g.6189C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*21C>G	ENSP00000453475.1:n.*21C>G
ENST00000699926.1:c.193C>G	ENSP00000514692.1:p.Leu65Val
ENST00000699934.1:c.159+31C>G	ENSP00000514697.1:n.159+31C>G
ENST00000699935.1:c.214C>G	ENSP00000514698.1:p.Leu72Val
ENST00000699936.1:c.124C>G	ENSP00000514699.1:p.Leu42Val
ENST00000699937.1:c.175C>G	ENSP00000514700.1:p.Leu59Val
ENST00000699938.1:c.159+31C>G	ENSP00000514701.1:n.159+31C>G
ENST00000699939.1:n.337C>G
ENST00000328848.6:c.190C>G MANE Select	ENSP00000332198.5:p.Leu64Val
ENST00000328848.5:c.190C>G	ENSP00000332198.4:p.Leu64Val
ENST00000557912.1:c.*21C>G	ENSP00000453475.1:n.*21C>G
NM_018648.3:c.190C>G , LRG_345t1:c.190C>G	NP_061118.1:p.Leu64Val
NM_018648.4:c.190C>G MANE Select	NP_061118.1:p.Leu64Val