Canonical Allele Identifier: CA2459737442
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475243G= , CM000685.2:g.134475243G= GRCh38
NC_000023.10:g.133609273G= , CM000685.1:g.133609273G= GRCh37
NC_000023.9:g.133436939G= NCBI36
NG_012329.1:g.20099G=
NG_012329.2:g.20099G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.197G= MANE Select ENSP00000298556.7:p.Cys66=
ENST00000298556.7:c.197G= ENSP00000298556.7:p.Cys66=
ENST00000462974.5:n.355G=
ENST00000475720.1:n.155G=
NM_000194.2:c.197G= NP_000185.1:p.Cys66=
XM_011531328.1:c.215G= XP_011529630.1:p.Cys72=
NM_000194.3:c.197G= MANE Select NP_000185.1:p.Cys66=