Canonical Allele Identifier: CA7464761

Gene: NOP10

Linked Data

• dbSNP Id: rs762158306
• ExAC: 15:34634178 A / G
• gnomAD v2: 15-34634178-A-G
• gnomAD v4: 15-34341977-A-G
• MyVariant Identifiers: chr15:g.34634178A>G (hg19) ; chr15:g.34341977A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341977A>G , CM000677.2:g.34341977A>G	GRCh38
NC_000015.9:g.34634178A>G , CM000677.1:g.34634178A>G	GRCh37
NC_000015.8:g.32421470A>G	NCBI36
NG_007951.1:g.1088T>C , LRG_270:g.1088T>C
NG_011562.1:g.6185T>C , LRG_345:g.6185T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*17T>C	ENSP00000453475.1:n.*17T>C
ENST00000699926.1:c.189T>C	ENSP00000514692.1:p.Pro63=
ENST00000699934.1:c.159+27T>C	ENSP00000514697.1:n.159+27T>C
ENST00000699935.1:c.210T>C	ENSP00000514698.1:p.Pro70=
ENST00000699936.1:c.120T>C	ENSP00000514699.1:p.Pro40=
ENST00000699937.1:c.171T>C	ENSP00000514700.1:p.Pro57=
ENST00000699938.1:c.159+27T>C	ENSP00000514701.1:n.159+27T>C
ENST00000699939.1:n.333T>C
ENST00000328848.6:c.186T>C MANE Select	ENSP00000332198.5:p.Pro62=
ENST00000328848.5:c.186T>C	ENSP00000332198.4:p.Pro62=
ENST00000557912.1:c.*17T>C	ENSP00000453475.1:n.*17T>C
NM_018648.3:c.186T>C , LRG_345t1:c.186T>C	NP_061118.1:p.Pro62=
NM_018648.4:c.186T>C MANE Select	NP_061118.1:p.Pro62=