Canonical Allele Identifier: CA2450373714

Gene: PRPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.107640957C= , CM000685.2:g.107640957C=	GRCh38
NC_000023.10:g.106884187C= , CM000685.1:g.106884187C=	GRCh37
NC_000023.9:g.106770843C=	NCBI36
NG_008407.1:g.17534C= , LRG_264:g.17534C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372418.4:c.307-1409C=	ENSP00000361495.2:n.307-1409C=
ENST00000372435.10:c.362C= MANE Select	ENSP00000361512.4:p.Ala121=
ENST00000643795.2:c.362C=	ENSP00000496286.1:p.Ala121=
ENST00000644642.1:c.123-4220C=	ENSP00000495493.1:n.123-4220C=
ENST00000645903.1:n.456C=
ENST00000674525.1:n.447C=
ENST00000674826.1:c.*55C=	ENSP00000502278.1:n.*55C=
ENST00000675046.1:c.184+1479C=
ENST00000675720.1:c.238C=
ENST00000676092.1:c.358+4C=	ENSP00000502780.1:n.358+4C=
ENST00000372418.2:c.106-1409C=	ENSP00000361495.1:n.106-1409C=
ENST00000372419.3:c.362C=	ENSP00000361496.3:p.Ala121=
ENST00000372428.8:c.-82-4220C=	ENSP00000361505.5:n.-82-4220C=
ENST00000372435.8:c.362C=	ENSP00000361512.4:p.Ala121=
NM_001204402.1:c.-82-4220C=	NP_001191331.1:n.-82-4220C=
NM_002764.3:c.362C= , LRG_264t1:c.362C=	NP_002755.1:p.Ala121=
NM_002764.4:c.362C= MANE Select	NP_002755.1:p.Ala121=
NM_001204402.2:c.-82-4220C=	NP_001191331.1:n.-82-4220C=