Canonical Allele Identifier: CA3764983

Gene: RPS10 RPS10-NUDT3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34417525C>T , CM000668.2:g.34417525C>T	GRCh38
NC_000006.11:g.34385302C>T , CM000668.1:g.34385302C>T	GRCh37
NC_000006.10:g.34493280C>T	NCBI36
NG_023200.1:g.13575G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001014.5:c.479G>A (RPS10) MANE Select	NP_001005.1:p.Arg160His
ENST00000648437.1:c.479G>A (RPS10) MANE Select	ENSP00000497917.1:p.Arg160His
NM_001014.4:c.479G>A (RPS10)	NP_001005.1:p.Arg160His
NM_001202470.2:c.456+844G>A (RPS10-NUDT3)	NP_001189399.1:n.456+844G>A
NM_001202470.3:c.456+844G>A (RPS10-NUDT3)	NP_001189399.1:n.456+844G>A
NM_001203245.2:c.479G>A (RPS10)	NP_001190174.1:p.Arg160His
NM_001203245.3:c.479G>A (RPS10)	NP_001190174.1:p.Arg160His
NM_001204091.1:c.479G>A (RPS10)	NP_001191020.1:p.Arg160His
NM_001204091.2:c.479G>A (RPS10)	NP_001191020.1:p.Arg160His
ENST00000326199.12:c.479G>A (RPS10)	ENSP00000347271.6:p.Arg160His
ENST00000344700.7:c.579G>A (RPS10)	ENSP00000363169.1:n.579G>A
ENST00000344700.8:c.*60G>A (RPS10)	ENSP00000363169.1:n.*60G>A
ENST00000464218.5:n.544G>A (RPS10)
ENST00000467531.5:n.706G>A (RPS10)
ENST00000494077.5:n.710G>A (RPS10)
ENST00000605528.1:c.456+844G>A (RPS10-NUDT3)	ENSP00000475027.1:n.456+844G>A
ENST00000605528.2:c.383+844G>A (RPS10-NUDT3)
ENST00000621356.2:c.479G>A (RPS10)	ENSP00000481646.1:p.Arg160His
ENST00000621356.3:c.479G>A (RPS10)	ENSP00000481646.1:p.Arg160His
ENST00000639725.1:c.456+844G>A (RPS10-NUDT3)	ENSP00000492441.1:n.456+844G>A
ENST00000639877.1:c.456+844G>A (RPS10-NUDT3)	ENSP00000491891.1:n.456+844G>A
ENST00000644393.1:c.542G>A (RPS10)	ENSP00000496022.1:p.Arg181His
ENST00000644700.1:c.*658G>A (RPS10)	ENSP00000495142.1:n.*658G>A