Canonical Allele Identifier: CA2450376200

Gene: PRPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.107649923C= , CM000685.2:g.107649923C=	GRCh38
NC_000023.10:g.106893153C= , CM000685.1:g.106893153C=	GRCh37
NC_000023.9:g.106779809C=	NCBI36
NG_008407.1:g.26500C= , LRG_264:g.26500C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372418.4:c.766-17C=	ENSP00000361495.2:n.766-17C=
ENST00000372428.9:c.248-17C=
ENST00000372435.10:c.865-17C= MANE Select	ENSP00000361512.4:n.865-17C=
ENST00000643795.2:c.802-655C=	ENSP00000496286.1:n.802-655C=
ENST00000644642.1:c.*334-17C=	ENSP00000495493.1:n.*334-17C=
ENST00000674826.1:c.*558-17C=	ENSP00000502278.1:n.*558-17C=
ENST00000675353.1:c.457-17C=
ENST00000675875.1:c.22-693C=
ENST00000676092.1:c.359-17C=	ENSP00000502780.1:n.359-17C=
ENST00000676365.1:c.433-17C=
ENST00000372418.2:c.565-17C=	ENSP00000361495.1:n.565-17C=
ENST00000372428.8:c.253-17C=	ENSP00000361505.5:n.253-17C=
ENST00000372435.8:c.865-17C=	ENSP00000361512.4:n.865-17C=
NM_001204402.1:c.253-17C=	NP_001191331.1:n.253-17C=
NM_002764.3:c.865-17C= , LRG_264t1:c.865-17C=	NP_002755.1:n.865-17C=
NM_002764.4:c.865-17C= MANE Select	NP_002755.1:n.865-17C=
NM_001204402.2:c.253-17C=	NP_001191331.1:n.253-17C=