Canonical Allele Identifier: CA414714161
Gene: HPRT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.133627540T>A (hg19) chrX:g.134493510T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134493510T>A , CM000685.2:g.134493510T>A GRCh38
NC_000023.10:g.133627540T>A , CM000685.1:g.133627540T>A GRCh37
NC_000023.9:g.133455206T>A NCBI36
NG_012329.1:g.38366T>A
NG_012329.2:g.38366T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.405T>A MANE Select ENSP00000298556.7:p.Asp135Glu
ENST00000298556.7:c.405T>A ENSP00000298556.7:p.Asp135Glu
ENST00000462974.5:n.563T>A
ENST00000475720.1:n.363T>A
NM_000194.2:c.405T>A NP_000185.1:p.Asp135Glu
XM_011531328.1:c.423T>A XP_011529630.1:p.Asp141Glu
NM_000194.3:c.405T>A MANE Select NP_000185.1:p.Asp135Glu
Search 100 bp 5'
Search 100 bp 3'