Canonical Allele Identifier: CA2627640129

Gene: NOP10

Linked Data

• gnomAD v4: 15-34341964-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341964A>G , CM000677.2:g.34341964A>G	GRCh38
NC_000015.9:g.34634165A>G , CM000677.1:g.34634165A>G	GRCh37
NC_000015.8:g.32421457A>G	NCBI36
NG_007951.1:g.1101T>C , LRG_270:g.1101T>C
NG_011562.1:g.6198T>C , LRG_345:g.6198T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*30T>C	ENSP00000453475.1:n.*30T>C
ENST00000699926.1:c.*4T>C	ENSP00000514692.1:n.*4T>C
ENST00000699934.1:c.159+40T>C	ENSP00000514697.1:n.159+40T>C
ENST00000699935.1:c.*4T>C	ENSP00000514698.1:n.*4T>C
ENST00000699936.1:c.*4T>C	ENSP00000514699.1:n.*4T>C
ENST00000699937.1:c.*4T>C	ENSP00000514700.1:n.*4T>C
ENST00000699938.1:c.159+40T>C	ENSP00000514701.1:n.159+40T>C
ENST00000699939.1:n.346T>C
ENST00000328848.6:c.*4T>C MANE Select	ENSP00000332198.5:n.*4T>C
ENST00000328848.5:c.*4T>C	ENSP00000332198.4:n.*4T>C
ENST00000557912.1:c.*30T>C	ENSP00000453475.1:n.*30T>C
NM_018648.3:c.*4T>C , LRG_345t1:c.*4T>C	NP_061118.1:n.*4T>C
NM_018648.4:c.*4T>C MANE Select	NP_061118.1:n.*4T>C