Canonical Allele Identifier: CA2459737420
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475174T= , CM000685.2:g.134475174T= GRCh38
NC_000023.10:g.133609204T= , CM000685.1:g.133609204T= GRCh37
NC_000023.9:g.133436870T= NCBI36
NG_012329.1:g.20030T=
NG_012329.2:g.20030T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135-7T= MANE Select ENSP00000298556.7:n.135-7T=
ENST00000298556.7:c.135-7T= ENSP00000298556.7:n.135-7T=
ENST00000462974.5:n.293-7T=
ENST00000475720.1:n.93-7T=
NM_000194.2:c.135-7T= NP_000185.1:n.135-7T=
XM_011531328.1:c.153-7T= XP_011529630.1:n.153-7T=
NM_000194.3:c.135-7T= MANE Select NP_000185.1:n.135-7T=