Canonical Allele Identifier: CA391622018

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634215T>A (hg19) ; chr15:g.34342014T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342014T>A , CM000677.2:g.34342014T>A	GRCh38
NC_000015.9:g.34634215T>A , CM000677.1:g.34634215T>A	GRCh37
NC_000015.8:g.32421507T>A	NCBI36
NG_007951.1:g.1051A>T , LRG_270:g.1051A>T
NG_011562.1:g.6148A>T , LRG_345:g.6148A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.91A>T	ENSP00000453475.1:p.Asn31Tyr
ENST00000699926.1:c.152A>T	ENSP00000514692.1:p.Lys51Ile
ENST00000699934.1:c.149A>T	ENSP00000514697.1:p.Lys50Ile
ENST00000699935.1:c.173A>T	ENSP00000514698.1:p.Lys58Ile
ENST00000699936.1:c.83A>T	ENSP00000514699.1:p.Lys28Ile
ENST00000699937.1:c.134A>T	ENSP00000514700.1:p.Lys45Ile
ENST00000699938.1:c.149A>T	ENSP00000514701.1:p.Lys50Ile
ENST00000699939.1:n.296A>T
ENST00000328848.6:c.149A>T MANE Select	ENSP00000332198.5:p.Lys50Ile
ENST00000328848.5:c.149A>T	ENSP00000332198.4:p.Lys50Ile
ENST00000557912.1:c.91A>T	ENSP00000453475.1:p.Asn31Tyr
NM_018648.3:c.149A>T , LRG_345t1:c.149A>T	NP_061118.1:p.Lys50Ile
NM_018648.4:c.149A>T MANE Select	NP_061118.1:p.Lys50Ile