Canonical Allele Identifier: CA2694742193
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475062_134475071del , CM000685.2:g.134475062_134475071del GRCh38
NC_000023.10:g.133609092_133609101del , CM000685.1:g.133609092_133609101del GRCh37
NC_000023.9:g.133436758_133436767del NCBI36
NG_012329.1:g.19918_19927del
NG_012329.2:g.19918_19927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-119_135-110del MANE Select ENSP00000298556.7:n.135-119_135-110del
ENST00000298556.7:c.135-119_135-110del ENSP00000298556.7:n.135-119_135-110del
ENST00000462974.5:n.293-119_293-110del
ENST00000475720.1:n.93-119_93-110del
NM_000194.2:c.135-119_135-110del NP_000185.1:n.135-119_135-110del
XM_011531328.1:c.153-119_153-110del XP_011529630.1:n.153-119_153-110del
NM_000194.3:c.135-119_135-110del MANE Select NP_000185.1:n.135-119_135-110del