Canonical Allele Identifier: CA2450373238
Gene: PRPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.107639235G= , CM000685.2:g.107639235G= GRCh38
NC_000023.10:g.106882465G= , CM000685.1:g.106882465G= GRCh37
NC_000023.9:g.106769121G= NCBI36
NG_008407.1:g.15812G= , LRG_264:g.15812G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372418.4:c.123-60G= ENSP00000361495.2:n.123-60G=
ENST00000372435.10:c.123-60G= MANE Select ENSP00000361512.4:n.123-60G=
ENST00000643795.2:c.123-60G= ENSP00000496286.1:n.123-60G=
ENST00000644642.1:c.123-5942G= ENSP00000495493.1:n.123-5942G=
ENST00000645638.1:c.*92-60G= ENSP00000496554.1:n.*92-60G=
ENST00000645903.1:n.217-60G=
ENST00000674525.1:n.208-60G=
ENST00000674826.1:c.123-1667G= ENSP00000502278.1:n.123-1667G=
ENST00000674843.1:c.225-60G= ENSP00000502260.1:n.225-60G=
ENST00000675304.1:n.56-60G=
ENST00000676092.1:c.123-60G= ENSP00000502780.1:n.123-60G=
ENST00000372419.3:c.123-60G= ENSP00000361496.3:n.123-60G=
ENST00000372428.8:c.-82-5942G= ENSP00000361505.5:n.-82-5942G=
ENST00000372435.8:c.123-60G= ENSP00000361512.4:n.123-60G=
NM_001204402.1:c.-82-5942G= NP_001191331.1:n.-82-5942G=
NM_002764.3:c.123-60G= , LRG_264t1:c.123-60G= NP_002755.1:n.123-60G=
NM_002764.4:c.123-60G= MANE Select NP_002755.1:n.123-60G=
NM_001204402.2:c.-82-5942G= NP_001191331.1:n.-82-5942G=