Canonical Allele Identifier: CA2459743319
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134493390T= , CM000685.2:g.134493390T= GRCh38
NC_000023.10:g.133627420T= , CM000685.1:g.133627420T= GRCh37
NC_000023.9:g.133455086T= NCBI36
NG_012329.1:g.38246T=
NG_012329.2:g.38246T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.403-118T= MANE Select ENSP00000298556.7:n.403-118T=
ENST00000298556.7:c.403-118T= ENSP00000298556.7:n.403-118T=
ENST00000462974.5:n.561-118T=
ENST00000475720.1:n.361-118T=
NM_000194.2:c.403-118T= NP_000185.1:n.403-118T=
XM_011531328.1:c.421-118T= XP_011529630.1:n.421-118T=
NM_000194.3:c.403-118T= MANE Select NP_000185.1:n.403-118T=
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