Canonical Allele Identifier: CA2450373258

Gene: PRPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.107639326G= , CM000685.2:g.107639326G=	GRCh38
NC_000023.10:g.106882556G= , CM000685.1:g.106882556G=	GRCh37
NC_000023.9:g.106769212G=	NCBI36
NG_008407.1:g.15903G= , LRG_264:g.15903G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372418.4:c.154G=	ENSP00000361495.2:p.Asp52=
ENST00000372435.10:c.154G= MANE Select	ENSP00000361512.4:p.Asp52=
ENST00000643795.2:c.154G=	ENSP00000496286.1:p.Asp52=
ENST00000644642.1:c.123-5851G=	ENSP00000495493.1:n.123-5851G=
ENST00000645638.1:c.*123G=	ENSP00000496554.1:n.*123G=
ENST00000645903.1:n.248G=
ENST00000674525.1:n.239G=
ENST00000674826.1:c.123-1576G=	ENSP00000502278.1:n.123-1576G=
ENST00000674843.1:c.256G=	ENSP00000502260.1:n.256G=
ENST00000675046.1:c.32G=
ENST00000675304.1:n.87G=
ENST00000675720.1:c.32G=
ENST00000676092.1:c.154G=	ENSP00000502780.1:p.Asp52=
ENST00000372419.3:c.154G=	ENSP00000361496.3:p.Asp52=
ENST00000372428.8:c.-82-5851G=	ENSP00000361505.5:n.-82-5851G=
ENST00000372435.8:c.154G=	ENSP00000361512.4:p.Asp52=
NM_001204402.1:c.-82-5851G=	NP_001191331.1:n.-82-5851G=
NM_002764.3:c.154G= , LRG_264t1:c.154G=	NP_002755.1:p.Asp52=
NM_002764.4:c.154G= MANE Select	NP_002755.1:p.Asp52=
NM_001204402.2:c.-82-5851G=	NP_001191331.1:n.-82-5851G=