Canonical Allele Identifier: CA414711826
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475179A>T , CM000685.2:g.134475179A>T GRCh38
NC_000023.10:g.133609209A>T , CM000685.1:g.133609209A>T GRCh37
NC_000023.9:g.133436875A>T NCBI36
NG_012329.1:g.20035A>T
NG_012329.2:g.20035A>T

Transcript Alleles

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