Canonical Allele Identifier: CA414711835
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475182A>G , CM000685.2:g.134475182A>G GRCh38
NC_000023.10:g.133609212A>G , CM000685.1:g.133609212A>G GRCh37
NC_000023.9:g.133436878A>G NCBI36
NG_012329.1:g.20038A>G
NG_012329.2:g.20038A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.136A>G MANE Select ENSP00000298556.7:p.Thr46Ala
ENST00000298556.7:c.136A>G ENSP00000298556.7:p.Thr46Ala
ENST00000462974.5:n.294A>G
ENST00000475720.1:n.94A>G
NM_000194.2:c.136A>G NP_000185.1:p.Thr46Ala
XM_011531328.1:c.154A>G XP_011529630.1:p.Thr52Ala
NM_000194.3:c.136A>G MANE Select NP_000185.1:p.Thr46Ala