Canonical Allele Identifier: CA391622092

Gene: NOP10

Linked Data

• MyVariant Identifiers: chr15:g.34634241G>T (hg19) ; chr15:g.34342040G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.34342040G>T , CM000677.2:g.34342040G>T	GRCh38
NC_000015.9:g.34634241G>T , CM000677.1:g.34634241G>T	GRCh37
NC_000015.8:g.32421533G>T	NCBI36
NG_007951.1:g.1025C>A , LRG_270:g.1025C>A
NG_011562.1:g.6122C>A , LRG_345:g.6122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557912.2:c.65C>A	ENSP00000453475.1:p.Thr22Asn
ENST00000699926.1:c.126C>A	ENSP00000514692.1:p.Tyr42Ter
ENST00000699934.1:c.123C>A	ENSP00000514697.1:p.Tyr41Ter
ENST00000699935.1:c.147C>A	ENSP00000514698.1:p.Tyr49Ter
ENST00000699936.1:c.57C>A	ENSP00000514699.1:p.Tyr19Ter
ENST00000699937.1:c.108C>A	ENSP00000514700.1:p.Tyr36Ter
ENST00000699938.1:c.123C>A	ENSP00000514701.1:p.Tyr41Ter
ENST00000699939.1:n.270C>A
ENST00000328848.6:c.123C>A MANE Select	ENSP00000332198.5:p.Tyr41Ter
ENST00000328848.5:c.123C>A	ENSP00000332198.4:p.Tyr41Ter
ENST00000557912.1:c.65C>A	ENSP00000453475.1:p.Thr22Asn
NM_018648.3:c.123C>A , LRG_345t1:c.123C>A	NP_061118.1:p.Tyr41Ter
NM_018648.4:c.123C>A MANE Select	NP_061118.1:p.Tyr41Ter