Canonical Allele Identifier: CA2579706161
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475082A>T , CM000685.2:g.134475082A>T GRCh38
NC_000023.10:g.133609112A>T , CM000685.1:g.133609112A>T GRCh37
NC_000023.9:g.133436778A>T NCBI36
NG_012329.1:g.19938A>T
NG_012329.2:g.19938A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-99A>T MANE Select ENSP00000298556.7:n.135-99A>T
ENST00000298556.7:c.135-99A>T ENSP00000298556.7:n.135-99A>T
ENST00000462974.5:n.293-99A>T
ENST00000475720.1:n.93-99A>T
NM_000194.2:c.135-99A>T NP_000185.1:n.135-99A>T
XM_011531328.1:c.153-99A>T XP_011529630.1:n.153-99A>T
NM_000194.3:c.135-99A>T MANE Select NP_000185.1:n.135-99A>T