Canonical Allele Identifier: CA2459737411
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475139T= , CM000685.2:g.134475139T= GRCh38
NC_000023.10:g.133609169T= , CM000685.1:g.133609169T= GRCh37
NC_000023.9:g.133436835T= NCBI36
NG_012329.1:g.19995T=
NG_012329.2:g.19995T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135-42T= MANE Select ENSP00000298556.7:n.135-42T=
ENST00000298556.7:c.135-42T= ENSP00000298556.7:n.135-42T=
ENST00000462974.5:n.293-42T=
ENST00000475720.1:n.93-42T=
NM_000194.2:c.135-42T= NP_000185.1:n.135-42T=
XM_011531328.1:c.153-42T= XP_011529630.1:n.153-42T=
NM_000194.3:c.135-42T= MANE Select NP_000185.1:n.135-42T=
Search 100 bp 5'
Search 100 bp 3'