Canonical Allele Identifier: CA391621933

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634180G>C (hg19) ; chr15:g.34341979G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341979G>C , CM000677.2:g.34341979G>C	GRCh38
NC_000015.9:g.34634180G>C , CM000677.1:g.34634180G>C	GRCh37
NC_000015.8:g.32421472G>C	NCBI36
NG_007951.1:g.1086C>G , LRG_270:g.1086C>G
NG_011562.1:g.6183C>G , LRG_345:g.6183C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*15C>G	ENSP00000453475.1:n.*15C>G
ENST00000699926.1:c.187C>G	ENSP00000514692.1:p.Pro63Ala
ENST00000699934.1:c.159+25C>G	ENSP00000514697.1:n.159+25C>G
ENST00000699935.1:c.208C>G	ENSP00000514698.1:p.Pro70Ala
ENST00000699936.1:c.118C>G	ENSP00000514699.1:p.Pro40Ala
ENST00000699937.1:c.169C>G	ENSP00000514700.1:p.Pro57Ala
ENST00000699938.1:c.159+25C>G	ENSP00000514701.1:n.159+25C>G
ENST00000699939.1:n.331C>G
ENST00000328848.6:c.184C>G MANE Select	ENSP00000332198.5:p.Pro62Ala
ENST00000328848.5:c.184C>G	ENSP00000332198.4:p.Pro62Ala
ENST00000557912.1:c.*15C>G	ENSP00000453475.1:n.*15C>G
NM_018648.3:c.184C>G , LRG_345t1:c.184C>G	NP_061118.1:p.Pro62Ala
NM_018648.4:c.184C>G MANE Select	NP_061118.1:p.Pro62Ala