Canonical Allele Identifier: CA2579706171
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475128A>G , CM000685.2:g.134475128A>G GRCh38
NC_000023.10:g.133609158A>G , CM000685.1:g.133609158A>G GRCh37
NC_000023.9:g.133436824A>G NCBI36
NG_012329.1:g.19984A>G
NG_012329.2:g.19984A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-53A>G MANE Select ENSP00000298556.7:n.135-53A>G
ENST00000298556.7:c.135-53A>G ENSP00000298556.7:n.135-53A>G
ENST00000462974.5:n.293-53A>G
ENST00000475720.1:n.93-53A>G
NM_000194.2:c.135-53A>G NP_000185.1:n.135-53A>G
XM_011531328.1:c.153-53A>G XP_011529630.1:n.153-53A>G
NM_000194.3:c.135-53A>G MANE Select NP_000185.1:n.135-53A>G