Canonical Allele Identifier: CA2694407235

Gene: PRPS1

Linked Data

• gnomAD v4: X-107639253-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.107639255dup , CM000685.2:g.107639255dup	GRCh38
NC_000023.10:g.106882485dup , CM000685.1:g.106882485dup	GRCh37
NC_000023.9:g.106769141dup	NCBI36
NG_008407.1:g.15832dup , LRG_264:g.15832dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000372418.4:c.123-40dup	ENSP00000361495.2:n.123-40dup
ENST00000372435.10:c.123-40dup MANE Select	ENSP00000361512.4:n.123-40dup
ENST00000643795.2:c.123-40dup	ENSP00000496286.1:n.123-40dup
ENST00000644642.1:c.123-5922dup	ENSP00000495493.1:n.123-5922dup
ENST00000645638.1:c.*92-40dup	ENSP00000496554.1:n.*92-40dup
ENST00000645903.1:n.217-40dup
ENST00000674525.1:n.208-40dup
ENST00000674826.1:c.123-1647dup	ENSP00000502278.1:n.123-1647dup
ENST00000674843.1:c.225-40dup	ENSP00000502260.1:n.225-40dup
ENST00000675304.1:n.56-40dup
ENST00000676092.1:c.123-40dup	ENSP00000502780.1:n.123-40dup
ENST00000372419.3:c.123-40dup	ENSP00000361496.3:n.123-40dup
ENST00000372428.8:c.-82-5922dup	ENSP00000361505.5:n.-82-5922dup
ENST00000372435.8:c.123-40dup	ENSP00000361512.4:n.123-40dup
NM_001204402.1:c.-82-5922dup	NP_001191331.1:n.-82-5922dup
NM_002764.3:c.123-40dup , LRG_264t1:c.123-40dup	NP_002755.1:n.123-40dup
NM_002764.4:c.123-40dup MANE Select	NP_002755.1:n.123-40dup
NM_001204402.2:c.-82-5922dup	NP_001191331.1:n.-82-5922dup