Canonical Allele Identifier: CA2459743338
Gene: HPRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134493491G= , CM000685.2:g.134493491G= GRCh38
NC_000023.10:g.133627521G= , CM000685.1:g.133627521G= GRCh37
NC_000023.9:g.133455187G= NCBI36
NG_012329.1:g.38347G=
NG_012329.2:g.38347G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.403-17G= MANE Select ENSP00000298556.7:n.403-17G=
ENST00000298556.7:c.403-17G= ENSP00000298556.7:n.403-17G=
ENST00000462974.5:n.561-17G=
ENST00000475720.1:n.361-17G=
NM_000194.2:c.403-17G= NP_000185.1:n.403-17G=
XM_011531328.1:c.421-17G= XP_011529630.1:n.421-17G=
NM_000194.3:c.403-17G= MANE Select NP_000185.1:n.403-17G=
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