Canonical Allele Identifier: CA2459741104
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134486475C= , CM000685.2:g.134486475C= GRCh38
NC_000023.10:g.133620505C= , CM000685.1:g.133620505C= GRCh37
NC_000023.9:g.133448171C= NCBI36
NG_012329.1:g.31331C=
NG_012329.2:g.31331C=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.329C= MANE Select ENSP00000298556.7:p.Ser110=
ENST00000298556.7:c.329C= ENSP00000298556.7:p.Ser110=
ENST00000462974.5:n.487C=
ENST00000475720.1:n.287C=
NM_000194.2:c.329C= NP_000185.1:p.Ser110=
XM_011531328.1:c.347C= XP_011529630.1:p.Ser116=
NM_000194.3:c.329C= MANE Select NP_000185.1:p.Ser110=