Canonical Allele Identifier: CA489409932

Gene: NOP10

Linked Data

• gnomAD v4: 15-34341977-A-T
• MyVariant Identifiers: chr15:g.34634178A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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