Canonical Allele Identifier: CA2450373252
Gene: PRPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.107639276C= , CM000685.2:g.107639276C= GRCh38
NC_000023.10:g.106882506C= , CM000685.1:g.106882506C= GRCh37
NC_000023.9:g.106769162C= NCBI36
NG_008407.1:g.15853C= , LRG_264:g.15853C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372418.4:c.123-19C= ENSP00000361495.2:n.123-19C=
ENST00000372435.10:c.123-19C= MANE Select ENSP00000361512.4:n.123-19C=
ENST00000643795.2:c.123-19C= ENSP00000496286.1:n.123-19C=
ENST00000644642.1:c.123-5901C= ENSP00000495493.1:n.123-5901C=
ENST00000645638.1:c.*92-19C= ENSP00000496554.1:n.*92-19C=
ENST00000645903.1:n.217-19C=
ENST00000674525.1:n.208-19C=
ENST00000674826.1:c.123-1626C= ENSP00000502278.1:n.123-1626C=
ENST00000674843.1:c.225-19C= ENSP00000502260.1:n.225-19C=
ENST00000675304.1:n.56-19C=
ENST00000676092.1:c.123-19C= ENSP00000502780.1:n.123-19C=
ENST00000372419.3:c.123-19C= ENSP00000361496.3:n.123-19C=
ENST00000372428.8:c.-82-5901C= ENSP00000361505.5:n.-82-5901C=
ENST00000372435.8:c.123-19C= ENSP00000361512.4:n.123-19C=
NM_001204402.1:c.-82-5901C= NP_001191331.1:n.-82-5901C=
NM_002764.3:c.123-19C= , LRG_264t1:c.123-19C= NP_002755.1:n.123-19C=
NM_002764.4:c.123-19C= MANE Select NP_002755.1:n.123-19C=
NM_001204402.2:c.-82-5901C= NP_001191331.1:n.-82-5901C=