Canonical Allele Identifier: CA2627640072

Gene: NOP10

Linked Data

• gnomAD v4: 15-34341869-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341869G>T , CM000677.2:g.34341869G>T	GRCh38
NC_000015.9:g.34634070G>T , CM000677.1:g.34634070G>T	GRCh37
NC_000015.8:g.32421362G>T	NCBI36
NG_007951.1:g.1196C>A , LRG_270:g.1196C>A
NG_011562.1:g.6293C>A , LRG_345:g.6293C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.*125C>A	ENSP00000453475.1:n.*125C>A
ENST00000699926.1:c.*99C>A	ENSP00000514692.1:n.*99C>A
ENST00000699934.1:c.159+135C>A	ENSP00000514697.1:n.159+135C>A
ENST00000699935.1:c.*99C>A	ENSP00000514698.1:n.*99C>A
ENST00000699936.1:c.*99C>A	ENSP00000514699.1:n.*99C>A
ENST00000699937.1:c.*99C>A	ENSP00000514700.1:n.*99C>A
ENST00000699938.1:c.*43C>A	ENSP00000514701.1:n.*43C>A
ENST00000699939.1:n.441C>A
ENST00000328848.6:c.*99C>A MANE Select	ENSP00000332198.5:n.*99C>A
ENST00000328848.5:c.*99C>A	ENSP00000332198.4:n.*99C>A
ENST00000557912.1:c.*125C>A	ENSP00000453475.1:n.*125C>A
NM_018648.3:c.*99C>A , LRG_345t1:c.*99C>A	NP_061118.1:n.*99C>A
NM_018648.4:c.*99C>A MANE Select	NP_061118.1:n.*99C>A