Canonical Allele Identifier: CA7464760

Gene: NOP10

Linked Data

• dbSNP Id: rs776538895
• ExAC: 15:34634174 G / A
• gnomAD v2: 15-34634174-G-A
• gnomAD v4: 15-34341973-G-A
• MyVariant Identifiers: chr15:g.34634174G>A (hg19) ; chr15:g.34341973G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341973G>A , CM000677.2:g.34341973G>A	GRCh38
NC_000015.9:g.34634174G>A , CM000677.1:g.34634174G>A	GRCh37
NC_000015.8:g.32421466G>A	NCBI36
NG_007951.1:g.1092C>T , LRG_270:g.1092C>T
NG_011562.1:g.6189C>T , LRG_345:g.6189C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*21C>T	ENSP00000453475.1:n.*21C>T
ENST00000699926.1:c.193C>T	ENSP00000514692.1:p.Leu65Phe
ENST00000699934.1:c.159+31C>T	ENSP00000514697.1:n.159+31C>T
ENST00000699935.1:c.214C>T	ENSP00000514698.1:p.Leu72Phe
ENST00000699936.1:c.124C>T	ENSP00000514699.1:p.Leu42Phe
ENST00000699937.1:c.175C>T	ENSP00000514700.1:p.Leu59Phe
ENST00000699938.1:c.159+31C>T	ENSP00000514701.1:n.159+31C>T
ENST00000699939.1:n.337C>T
ENST00000328848.6:c.190C>T MANE Select	ENSP00000332198.5:p.Leu64Phe
ENST00000328848.5:c.190C>T	ENSP00000332198.4:p.Leu64Phe
ENST00000557912.1:c.*21C>T	ENSP00000453475.1:n.*21C>T
NM_018648.3:c.190C>T , LRG_345t1:c.190C>T	NP_061118.1:p.Leu64Phe
NM_018648.4:c.190C>T MANE Select	NP_061118.1:p.Leu64Phe