Canonical Allele Identifier: CA2459737447
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475265A= , CM000685.2:g.134475265A= GRCh38
NC_000023.10:g.133609295A= , CM000685.1:g.133609295A= GRCh37
NC_000023.9:g.133436961A= NCBI36
NG_012329.1:g.20121A=
NG_012329.2:g.20121A=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.219A= MANE Select ENSP00000298556.7:p.Lys73=
ENST00000298556.7:c.219A= ENSP00000298556.7:p.Lys73=
ENST00000462974.5:n.377A=
ENST00000475720.1:n.177A=
NM_000194.2:c.219A= NP_000185.1:p.Lys73=
XM_011531328.1:c.237A= XP_011529630.1:p.Lys79=
NM_000194.3:c.219A= MANE Select NP_000185.1:p.Lys73=