Canonical Allele Identifier: CA2459744833
Gene: HPRT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134498246A= , CM000685.2:g.134498246A= GRCh38
NC_000023.10:g.133632276A= , CM000685.1:g.133632276A= GRCh37
NC_000023.9:g.133459942A= NCBI36
NG_012329.1:g.43102A=
NG_012329.2:g.43102A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.486-144A= MANE Select ENSP00000298556.7:n.486-144A=
ENST00000298556.7:c.486-144A= ENSP00000298556.7:n.486-144A=
ENST00000462974.5:n.644-144A=
ENST00000475720.1:n.444-144A=
NM_000194.2:c.486-144A= NP_000185.1:n.486-144A=
XM_011531328.1:c.504-144A= XP_011529630.1:n.504-144A=
NM_000194.3:c.486-144A= MANE Select NP_000185.1:n.486-144A=
Search 100 bp 5'
Search 100 bp 3'