Canonical Allele Identifier: CA518650370
Gene: HPRT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.133627573G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134493543G>A , CM000685.2:g.134493543G>A GRCh38
NC_000023.10:g.133627573G>A , CM000685.1:g.133627573G>A GRCh37
NC_000023.9:g.133455239G>A NCBI36
NG_012329.1:g.38399G>A
NG_012329.2:g.38399G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.438G>A MANE Select ENSP00000298556.7:p.Leu146=
ENST00000298556.7:c.438G>A ENSP00000298556.7:p.Leu146=
ENST00000462974.5:n.596G>A
ENST00000475720.1:n.396G>A
NM_000194.2:c.438G>A NP_000185.1:p.Leu146=
XM_011531328.1:c.456G>A XP_011529630.1:p.Leu152=
NM_000194.3:c.438G>A MANE Select NP_000185.1:p.Leu146=
Search 100 bp 5'
Search 100 bp 3'