Canonical Allele Identifier: CA414712100
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475263A>T , CM000685.2:g.134475263A>T GRCh38
NC_000023.10:g.133609293A>T , CM000685.1:g.133609293A>T GRCh37
NC_000023.9:g.133436959A>T NCBI36
NG_012329.1:g.20119A>T
NG_012329.2:g.20119A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.217A>T MANE Select ENSP00000298556.7:p.Lys73Ter
ENST00000298556.7:c.217A>T ENSP00000298556.7:p.Lys73Ter
ENST00000462974.5:n.375A>T
ENST00000475720.1:n.175A>T
NM_000194.2:c.217A>T NP_000185.1:p.Lys73Ter
XM_011531328.1:c.235A>T XP_011529630.1:p.Lys79Ter
NM_000194.3:c.217A>T MANE Select NP_000185.1:p.Lys73Ter