Canonical Allele Identifier: CA414712108
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475266T>C , CM000685.2:g.134475266T>C GRCh38
NC_000023.10:g.133609296T>C , CM000685.1:g.133609296T>C GRCh37
NC_000023.9:g.133436962T>C NCBI36
NG_012329.1:g.20122T>C
NG_012329.2:g.20122T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.220T>C MANE Select ENSP00000298556.7:p.Phe74Leu
ENST00000298556.7:c.220T>C ENSP00000298556.7:p.Phe74Leu
ENST00000462974.5:n.378T>C
ENST00000475720.1:n.178T>C
NM_000194.2:c.220T>C NP_000185.1:p.Phe74Leu
XM_011531328.1:c.238T>C XP_011529630.1:p.Phe80Leu
NM_000194.3:c.220T>C MANE Select NP_000185.1:p.Phe74Leu