Canonical Allele Identifier: CA414711830
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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