Canonical Allele Identifier: CA391622029

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634218T>G (hg19) ; chr15:g.34342017T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342017T>G , CM000677.2:g.34342017T>G	GRCh38
NC_000015.9:g.34634218T>G , CM000677.1:g.34634218T>G	GRCh37
NC_000015.8:g.32421510T>G	NCBI36
NG_007951.1:g.1048A>C , LRG_270:g.1048A>C
NG_011562.1:g.6145A>C , LRG_345:g.6145A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.88A>C	ENSP00000453475.1:p.Arg30=
ENST00000699926.1:c.149A>C	ENSP00000514692.1:p.Lys50Thr
ENST00000699934.1:c.146A>C	ENSP00000514697.1:p.Lys49Thr
ENST00000699935.1:c.170A>C	ENSP00000514698.1:p.Lys57Thr
ENST00000699936.1:c.80A>C	ENSP00000514699.1:p.Lys27Thr
ENST00000699937.1:c.131A>C	ENSP00000514700.1:p.Lys44Thr
ENST00000699938.1:c.146A>C	ENSP00000514701.1:p.Lys49Thr
ENST00000699939.1:n.293A>C
ENST00000328848.6:c.146A>C MANE Select	ENSP00000332198.5:p.Lys49Thr
ENST00000328848.5:c.146A>C	ENSP00000332198.4:p.Lys49Thr
ENST00000557912.1:c.88A>C	ENSP00000453475.1:p.Arg30=
NM_018648.3:c.146A>C , LRG_345t1:c.146A>C	NP_061118.1:p.Lys49Thr
NM_018648.4:c.146A>C MANE Select	NP_061118.1:p.Lys49Thr