Canonical Allele Identifier: CA2459743310
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134493347C= , CM000685.2:g.134493347C= GRCh38
NC_000023.10:g.133627377C= , CM000685.1:g.133627377C= GRCh37
NC_000023.9:g.133455043C= NCBI36
NG_012329.1:g.38203C=
NG_012329.2:g.38203C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.403-161C= MANE Select ENSP00000298556.7:n.403-161C=
ENST00000298556.7:c.403-161C= ENSP00000298556.7:n.403-161C=
ENST00000462974.5:n.561-161C=
ENST00000475720.1:n.361-161C=
NM_000194.2:c.403-161C= NP_000185.1:n.403-161C=
XM_011531328.1:c.421-161C= XP_011529630.1:n.421-161C=
NM_000194.3:c.403-161C= MANE Select NP_000185.1:n.403-161C=
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