Canonical Allele Identifier: CA413804403
Gene: PRPS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.107639323G>A , CM000685.2:g.107639323G>A GRCh38
NC_000023.10:g.106882553G>A , CM000685.1:g.106882553G>A GRCh37
NC_000023.9:g.106769209G>A NCBI36
NG_008407.1:g.15900G>A , LRG_264:g.15900G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372418.4:c.151G>A ENSP00000361495.2:p.Glu51Lys
ENST00000372435.10:c.151G>A MANE Select ENSP00000361512.4:p.Glu51Lys
ENST00000643795.2:c.151G>A ENSP00000496286.1:p.Glu51Lys
ENST00000644642.1:c.123-5854G>A ENSP00000495493.1:n.123-5854G>A
ENST00000645638.1:c.*120G>A ENSP00000496554.1:n.*120G>A
ENST00000645903.1:n.245G>A
ENST00000674525.1:n.236G>A
ENST00000674826.1:c.123-1579G>A ENSP00000502278.1:n.123-1579G>A
ENST00000674843.1:c.253G>A ENSP00000502260.1:n.253G>A
ENST00000675046.1:c.29G>A
ENST00000675304.1:n.84G>A
ENST00000675720.1:c.29G>A
ENST00000676092.1:c.151G>A ENSP00000502780.1:p.Glu51Lys
ENST00000372419.3:c.151G>A ENSP00000361496.3:p.Glu51Lys
ENST00000372428.8:c.-82-5854G>A ENSP00000361505.5:n.-82-5854G>A
ENST00000372435.8:c.151G>A ENSP00000361512.4:p.Glu51Lys
NM_001204402.1:c.-82-5854G>A NP_001191331.1:n.-82-5854G>A
NM_002764.3:c.151G>A , LRG_264t1:c.151G>A NP_002755.1:p.Glu51Lys
NM_002764.4:c.151G>A MANE Select NP_002755.1:p.Glu51Lys
NM_001204402.2:c.-82-5854G>A NP_001191331.1:n.-82-5854G>A