Canonical Allele Identifier: CA2459743339
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134493496C= , CM000685.2:g.134493496C= GRCh38
NC_000023.10:g.133627526C= , CM000685.1:g.133627526C= GRCh37
NC_000023.9:g.133455192C= NCBI36
NG_012329.1:g.38352C=
NG_012329.2:g.38352C=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.403-12C= MANE Select ENSP00000298556.7:n.403-12C=
ENST00000298556.7:c.403-12C= ENSP00000298556.7:n.403-12C=
ENST00000462974.5:n.561-12C=
ENST00000475720.1:n.361-12C=
NM_000194.2:c.403-12C= NP_000185.1:n.403-12C=
XM_011531328.1:c.421-12C= XP_011529630.1:n.421-12C=
NM_000194.3:c.403-12C= MANE Select NP_000185.1:n.403-12C=
Search 100 bp 5'
Search 100 bp 3'