Canonical Allele Identifier: CA414712098
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475262T>G , CM000685.2:g.134475262T>G GRCh38
NC_000023.10:g.133609292T>G , CM000685.1:g.133609292T>G GRCh37
NC_000023.9:g.133436958T>G NCBI36
NG_012329.1:g.20118T>G
NG_012329.2:g.20118T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.216T>G MANE Select ENSP00000298556.7:p.Tyr72Ter
ENST00000298556.7:c.216T>G ENSP00000298556.7:p.Tyr72Ter
ENST00000462974.5:n.374T>G
ENST00000475720.1:n.174T>G
NM_000194.2:c.216T>G NP_000185.1:p.Tyr72Ter
XM_011531328.1:c.234T>G XP_011529630.1:p.Tyr78Ter
NM_000194.3:c.216T>G MANE Select NP_000185.1:p.Tyr72Ter