Canonical Allele Identifier: CA2459737393
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475071G= , CM000685.2:g.134475071G= GRCh38
NC_000023.10:g.133609101G= , CM000685.1:g.133609101G= GRCh37
NC_000023.9:g.133436767G= NCBI36
NG_012329.1:g.19927G=
NG_012329.2:g.19927G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-110G= MANE Select ENSP00000298556.7:n.135-110G=
ENST00000298556.7:c.135-110G= ENSP00000298556.7:n.135-110G=
ENST00000462974.5:n.293-110G=
ENST00000475720.1:n.93-110G=
NM_000194.2:c.135-110G= NP_000185.1:n.135-110G=
XM_011531328.1:c.153-110G= XP_011529630.1:n.153-110G=
NM_000194.3:c.135-110G= MANE Select NP_000185.1:n.135-110G=