Canonical Allele Identifier: CA414712073
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475251A>C , CM000685.2:g.134475251A>C GRCh38
NC_000023.10:g.133609281A>C , CM000685.1:g.133609281A>C GRCh37
NC_000023.9:g.133436947A>C NCBI36
NG_012329.1:g.20107A>C
NG_012329.2:g.20107A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.205A>C MANE Select ENSP00000298556.7:p.Lys69Gln
ENST00000298556.7:c.205A>C ENSP00000298556.7:p.Lys69Gln
ENST00000462974.5:n.363A>C
ENST00000475720.1:n.163A>C
NM_000194.2:c.205A>C NP_000185.1:p.Lys69Gln
XM_011531328.1:c.223A>C XP_011529630.1:p.Lys75Gln
NM_000194.3:c.205A>C MANE Select NP_000185.1:p.Lys69Gln