Canonical Allele Identifier: CA2823682814
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475076del , CM000685.2:g.134475076del GRCh38
NC_000023.10:g.133609106del , CM000685.1:g.133609106del GRCh37
NC_000023.9:g.133436772del NCBI36
NG_012329.1:g.19932del
NG_012329.2:g.19932del

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135-105del MANE Select ENSP00000298556.7:n.135-105del
ENST00000298556.7:c.135-105del ENSP00000298556.7:n.135-105del
ENST00000462974.5:n.293-105del
ENST00000475720.1:n.93-105del
NM_000194.2:c.135-105del NP_000185.1:n.135-105del
XM_011531328.1:c.153-105del XP_011529630.1:n.153-105del
NM_000194.3:c.135-105del MANE Select NP_000185.1:n.135-105del
Search 100 bp 5'
Search 100 bp 3'