Canonical Allele Identifier: CA2580101550
Gene: HPRT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138720
ClinVar RCV Id: RCV003041482

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475258del , CM000685.2:g.134475258del GRCh38
NC_000023.10:g.133609288del , CM000685.1:g.133609288del GRCh37
NC_000023.9:g.133436954del NCBI36
NG_012329.1:g.20114del
NG_012329.2:g.20114del

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.212del MANE Select ENSP00000298556.7:p.Gly71AlafsTer15
ENST00000298556.7:c.212del ENSP00000298556.7:p.Gly71AlafsTer15
ENST00000462974.5:n.370del
ENST00000475720.1:n.170del
NM_000194.2:c.212del NP_000185.1:p.Gly71AlafsTer15
XM_011531328.1:c.230del XP_011529630.1:p.Gly77AlafsTer15
NM_000194.3:c.212del MANE Select NP_000185.1:p.Gly71AlafsTer15