Canonical Allele Identifier: CA2579706182
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475250del , CM000685.2:g.134475250del GRCh38
NC_000023.10:g.133609280del , CM000685.1:g.133609280del GRCh37
NC_000023.9:g.133436946del NCBI36
NG_012329.1:g.20106del
NG_012329.2:g.20106del

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.204del MANE Select ENSP00000298556.7:p.Lys69ArgfsTer17
ENST00000298556.7:c.204del ENSP00000298556.7:p.Lys69ArgfsTer17
ENST00000462974.5:n.362del
ENST00000475720.1:n.162del
NM_000194.2:c.204del NP_000185.1:p.Lys69ArgfsTer17
XM_011531328.1:c.222del XP_011529630.1:p.Lys75ArgfsTer17
NM_000194.3:c.204del MANE Select NP_000185.1:p.Lys69ArgfsTer17
Search 100 bp 5'
Search 100 bp 3'