Canonical Allele Identifier: CA489409927

Gene: NOP10

Linked Data

• gnomAD v4: 15-34341974-G-A
• MyVariant Identifiers: chr15:g.34634175G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341974G>A , CM000677.2:g.34341974G>A	GRCh38
NC_000015.9:g.34634175G>A , CM000677.1:g.34634175G>A	GRCh37
NC_000015.8:g.32421467G>A	NCBI36
NG_007951.1:g.1091C>T , LRG_270:g.1091C>T
NG_011562.1:g.6188C>T , LRG_345:g.6188C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*20C>T	ENSP00000453475.1:n.*20C>T
ENST00000699926.1:c.192C>T	ENSP00000514692.1:p.Val64=
ENST00000699934.1:c.159+30C>T	ENSP00000514697.1:n.159+30C>T
ENST00000699935.1:c.213C>T	ENSP00000514698.1:p.Val71=
ENST00000699936.1:c.123C>T	ENSP00000514699.1:p.Val41=
ENST00000699937.1:c.174C>T	ENSP00000514700.1:p.Val58=
ENST00000699938.1:c.159+30C>T	ENSP00000514701.1:n.159+30C>T
ENST00000699939.1:n.336C>T
ENST00000328848.6:c.189C>T MANE Select	ENSP00000332198.5:p.Val63=
ENST00000328848.5:c.189C>T	ENSP00000332198.4:p.Val63=
ENST00000557912.1:c.*20C>T	ENSP00000453475.1:n.*20C>T
NM_018648.3:c.189C>T , LRG_345t1:c.189C>T	NP_061118.1:p.Val63=
NM_018648.4:c.189C>T MANE Select	NP_061118.1:p.Val63=