Canonical Allele Identifier: CA363885557

Gene: RPS10 RPS10-NUDT3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34417531C>T , CM000668.2:g.34417531C>T	GRCh38
NC_000006.11:g.34385308C>T , CM000668.1:g.34385308C>T	GRCh37
NC_000006.10:g.34493286C>T	NCBI36
NG_023200.1:g.13569G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001014.5:c.473G>A (RPS10) MANE Select	NP_001005.1:p.Arg158His
ENST00000648437.1:c.473G>A (RPS10) MANE Select	ENSP00000497917.1:p.Arg158His
NM_001014.4:c.473G>A (RPS10)	NP_001005.1:p.Arg158His
NM_001202470.2:c.456+838G>A (RPS10-NUDT3)	NP_001189399.1:n.456+838G>A
NM_001202470.3:c.456+838G>A (RPS10-NUDT3)	NP_001189399.1:n.456+838G>A
NM_001203245.2:c.473G>A (RPS10)	NP_001190174.1:p.Arg158His
NM_001203245.3:c.473G>A (RPS10)	NP_001190174.1:p.Arg158His
NM_001204091.1:c.473G>A (RPS10)	NP_001191020.1:p.Arg158His
NM_001204091.2:c.473G>A (RPS10)	NP_001191020.1:p.Arg158His
ENST00000326199.12:c.473G>A (RPS10)	ENSP00000347271.6:p.Arg158His
ENST00000344700.7:c.573G>A (RPS10)	ENSP00000363169.1:n.573G>A
ENST00000344700.8:c.*54G>A (RPS10)	ENSP00000363169.1:n.*54G>A
ENST00000464218.5:n.538G>A (RPS10)
ENST00000467531.5:n.700G>A (RPS10)
ENST00000494077.5:n.704G>A (RPS10)
ENST00000605528.1:c.456+838G>A (RPS10-NUDT3)	ENSP00000475027.1:n.456+838G>A
ENST00000605528.2:c.383+838G>A (RPS10-NUDT3)
ENST00000621356.2:c.473G>A (RPS10)	ENSP00000481646.1:p.Arg158His
ENST00000621356.3:c.473G>A (RPS10)	ENSP00000481646.1:p.Arg158His
ENST00000639725.1:c.456+838G>A (RPS10-NUDT3)	ENSP00000492441.1:n.456+838G>A
ENST00000639877.1:c.456+838G>A (RPS10-NUDT3)	ENSP00000491891.1:n.456+838G>A
ENST00000644393.1:c.536G>A (RPS10)	ENSP00000496022.1:p.Arg179His
ENST00000644700.1:c.*652G>A (RPS10)	ENSP00000495142.1:n.*652G>A