Canonical Allele Identifier: CA2459737418
Gene: HPRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475162C= , CM000685.2:g.134475162C= GRCh38
NC_000023.10:g.133609192C= , CM000685.1:g.133609192C= GRCh37
NC_000023.9:g.133436858C= NCBI36
NG_012329.1:g.20018C=
NG_012329.2:g.20018C=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135-19C= MANE Select ENSP00000298556.7:n.135-19C=
ENST00000298556.7:c.135-19C= ENSP00000298556.7:n.135-19C=
ENST00000462974.5:n.293-19C=
ENST00000475720.1:n.93-19C=
NM_000194.2:c.135-19C= NP_000185.1:n.135-19C=
XM_011531328.1:c.153-19C= XP_011529630.1:n.153-19C=
NM_000194.3:c.135-19C= MANE Select NP_000185.1:n.135-19C=