Canonical Allele Identifier: CA10485592

Gene: PRPS1

Linked Data

• dbSNP Id: rs367746767
• ExAC: X:106882495 T / G
• gnomAD v2: X-106882495-T-G
• gnomAD v3: X-107639265-T-G
• gnomAD v4: X-107639265-T-G
• MyVariant Identifiers: chrX:g.106882495T>G (hg19) ; chrX:g.107639265T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.107639265T>G , CM000685.2:g.107639265T>G	GRCh38
NC_000023.10:g.106882495T>G , CM000685.1:g.106882495T>G	GRCh37
NC_000023.9:g.106769151T>G	NCBI36
NG_008407.1:g.15842T>G , LRG_264:g.15842T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372418.4:c.123-30T>G	ENSP00000361495.2:n.123-30T>G
ENST00000372435.10:c.123-30T>G MANE Select	ENSP00000361512.4:n.123-30T>G
ENST00000643795.2:c.123-30T>G	ENSP00000496286.1:n.123-30T>G
ENST00000644642.1:c.123-5912T>G	ENSP00000495493.1:n.123-5912T>G
ENST00000645638.1:c.*92-30T>G	ENSP00000496554.1:n.*92-30T>G
ENST00000645903.1:n.217-30T>G
ENST00000674525.1:n.208-30T>G
ENST00000674826.1:c.123-1637T>G	ENSP00000502278.1:n.123-1637T>G
ENST00000674843.1:c.225-30T>G	ENSP00000502260.1:n.225-30T>G
ENST00000675304.1:n.56-30T>G
ENST00000676092.1:c.123-30T>G	ENSP00000502780.1:n.123-30T>G
ENST00000372419.3:c.123-30T>G	ENSP00000361496.3:n.123-30T>G
ENST00000372428.8:c.-82-5912T>G	ENSP00000361505.5:n.-82-5912T>G
ENST00000372435.8:c.123-30T>G	ENSP00000361512.4:n.123-30T>G
NM_001204402.1:c.-82-5912T>G	NP_001191331.1:n.-82-5912T>G
NM_002764.3:c.123-30T>G , LRG_264t1:c.123-30T>G	NP_002755.1:n.123-30T>G
NM_002764.4:c.123-30T>G MANE Select	NP_002755.1:n.123-30T>G
NM_001204402.2:c.-82-5912T>G	NP_001191331.1:n.-82-5912T>G