Canonical Allele Identifier: CA391621931

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634179G>T (hg19) ; chr15:g.34341978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34341978G>T , CM000677.2:g.34341978G>T	GRCh38
NC_000015.9:g.34634179G>T , CM000677.1:g.34634179G>T	GRCh37
NC_000015.8:g.32421471G>T	NCBI36
NG_007951.1:g.1087C>A , LRG_270:g.1087C>A
NG_011562.1:g.6184C>A , LRG_345:g.6184C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557912.2:c.*16C>A	ENSP00000453475.1:n.*16C>A
ENST00000699926.1:c.188C>A	ENSP00000514692.1:p.Pro63His
ENST00000699934.1:c.159+26C>A	ENSP00000514697.1:n.159+26C>A
ENST00000699935.1:c.209C>A	ENSP00000514698.1:p.Pro70His
ENST00000699936.1:c.119C>A	ENSP00000514699.1:p.Pro40His
ENST00000699937.1:c.170C>A	ENSP00000514700.1:p.Pro57His
ENST00000699938.1:c.159+26C>A	ENSP00000514701.1:n.159+26C>A
ENST00000699939.1:n.332C>A
ENST00000328848.6:c.185C>A MANE Select	ENSP00000332198.5:p.Pro62His
ENST00000328848.5:c.185C>A	ENSP00000332198.4:p.Pro62His
ENST00000557912.1:c.*16C>A	ENSP00000453475.1:n.*16C>A
NM_018648.3:c.185C>A , LRG_345t1:c.185C>A	NP_061118.1:p.Pro62His
NM_018648.4:c.185C>A MANE Select	NP_061118.1:p.Pro62His