Canonical Allele Identifier: CA391621992

Gene: NOP10

Linked Data

• gnomAD v4: 15-34342003-C-T
• MyVariant Identifiers: chr15:g.34634204C>T (hg19) ; chr15:g.34342003C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342003C>T , CM000677.2:g.34342003C>T	GRCh38
NC_000015.9:g.34634204C>T , CM000677.1:g.34634204C>T	GRCh37
NC_000015.8:g.32421496C>T	NCBI36
NG_007951.1:g.1062G>A , LRG_270:g.1062G>A
NG_011562.1:g.6159G>A , LRG_345:g.6159G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.102G>A	ENSP00000453475.1:p.Arg34=
ENST00000699926.1:c.163G>A	ENSP00000514692.1:p.Val55Met
ENST00000699934.1:c.159+1G>A	ENSP00000514697.1:n.159+1G>A
ENST00000699935.1:c.184G>A	ENSP00000514698.1:p.Val62Met
ENST00000699936.1:c.94G>A	ENSP00000514699.1:p.Val32Met
ENST00000699937.1:c.145G>A	ENSP00000514700.1:p.Val49Met
ENST00000699938.1:c.159+1G>A	ENSP00000514701.1:n.159+1G>A
ENST00000699939.1:n.307G>A
ENST00000328848.6:c.160G>A MANE Select	ENSP00000332198.5:p.Val54Met
ENST00000328848.5:c.160G>A	ENSP00000332198.4:p.Val54Met
ENST00000557912.1:c.102G>A	ENSP00000453475.1:p.Arg34=
NM_018648.3:c.160G>A , LRG_345t1:c.160G>A	NP_061118.1:p.Val54Met
NM_018648.4:c.160G>A MANE Select	NP_061118.1:p.Val54Met