Canonical Allele Identifier: CA414711832
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475181G>T , CM000685.2:g.134475181G>T GRCh38
NC_000023.10:g.133609211G>T , CM000685.1:g.133609211G>T GRCh37
NC_000023.9:g.133436877G>T NCBI36
NG_012329.1:g.20037G>T
NG_012329.2:g.20037G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135G>T MANE Select ENSP00000298556.7:p.Arg45Ser
ENST00000298556.7:c.135G>T ENSP00000298556.7:p.Arg45Ser
ENST00000462974.5:n.293G>T
ENST00000475720.1:n.93G>T
NM_000194.2:c.135G>T NP_000185.1:p.Arg45Ser
XM_011531328.1:c.153G>T XP_011529630.1:p.Arg51Ser
NM_000194.3:c.135G>T MANE Select NP_000185.1:p.Arg45Ser