Canonical Allele Identifier: CA2459737395
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475080A= , CM000685.2:g.134475080A= GRCh38
NG_012329.2:g.19936A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-101A= MANE Select ENSP00000298556.7:n.135-101A=
ENST00000298556.7:c.135-101A= ENSP00000298556.7:n.135-101A=
ENST00000462974.5:n.293-101A=
ENST00000475720.1:n.93-101A=
NM_000194.2:c.135-101A= NP_000185.1:n.135-101A=
XM_011531328.1:c.153-101A= XP_011529630.1:n.153-101A=
NM_000194.3:c.135-101A= MANE Select NP_000185.1:n.135-101A=