Canonical Allele Identifier: CA2694742265
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475170del , CM000685.2:g.134475170del GRCh38
NC_000023.10:g.133609200del , CM000685.1:g.133609200del GRCh37
NC_000023.9:g.133436866del NCBI36
NG_012329.1:g.20026del
NG_012329.2:g.20026del

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135-11del MANE Select ENSP00000298556.7:n.135-11del
ENST00000298556.7:c.135-11del ENSP00000298556.7:n.135-11del
ENST00000462974.5:n.293-11del
ENST00000475720.1:n.93-11del
NM_000194.2:c.135-11del NP_000185.1:n.135-11del
XM_011531328.1:c.153-11del XP_011529630.1:n.153-11del
NM_000194.3:c.135-11del MANE Select NP_000185.1:n.135-11del