Canonical Allele Identifier: CA413804555

Gene: PRPS1

Linked Data

• MyVariant Identifiers: chrX:g.106882566T>C (hg19) ; chrX:g.107639336T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.107639336T>C , CM000685.2:g.107639336T>C	GRCh38
NC_000023.10:g.106882566T>C , CM000685.1:g.106882566T>C	GRCh37
NC_000023.9:g.106769222T>C	NCBI36
NG_008407.1:g.15913T>C , LRG_264:g.15913T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372418.4:c.164T>C	ENSP00000361495.2:p.Ile55Thr
ENST00000372435.10:c.164T>C MANE Select	ENSP00000361512.4:p.Ile55Thr
ENST00000643795.2:c.164T>C	ENSP00000496286.1:p.Ile55Thr
ENST00000644642.1:c.123-5841T>C	ENSP00000495493.1:n.123-5841T>C
ENST00000645638.1:c.*133T>C	ENSP00000496554.1:n.*133T>C
ENST00000645903.1:n.258T>C
ENST00000674525.1:n.249T>C
ENST00000674826.1:c.123-1566T>C	ENSP00000502278.1:n.123-1566T>C
ENST00000674843.1:c.266T>C	ENSP00000502260.1:n.266T>C
ENST00000675046.1:c.42T>C
ENST00000675304.1:n.97T>C
ENST00000675720.1:c.42T>C
ENST00000676092.1:c.164T>C	ENSP00000502780.1:p.Ile55Thr
ENST00000372419.3:c.164T>C	ENSP00000361496.3:p.Ile55Thr
ENST00000372428.8:c.-82-5841T>C	ENSP00000361505.5:n.-82-5841T>C
ENST00000372435.8:c.164T>C	ENSP00000361512.4:p.Ile55Thr
NM_001204402.1:c.-82-5841T>C	NP_001191331.1:n.-82-5841T>C
NM_002764.3:c.164T>C , LRG_264t1:c.164T>C	NP_002755.1:p.Ile55Thr
NM_002764.4:c.164T>C MANE Select	NP_002755.1:p.Ile55Thr
NM_001204402.2:c.-82-5841T>C	NP_001191331.1:n.-82-5841T>C