Canonical Allele Identifier: CA414712067
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475246T>G , CM000685.2:g.134475246T>G GRCh38
NC_000023.10:g.133609276T>G , CM000685.1:g.133609276T>G GRCh37
NC_000023.9:g.133436942T>G NCBI36
NG_012329.1:g.20102T>G
NG_012329.2:g.20102T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.200T>G MANE Select ENSP00000298556.7:p.Val67Gly
ENST00000298556.7:c.200T>G ENSP00000298556.7:p.Val67Gly
ENST00000462974.5:n.358T>G
ENST00000475720.1:n.158T>G
NM_000194.2:c.200T>G NP_000185.1:p.Val67Gly
XM_011531328.1:c.218T>G XP_011529630.1:p.Val73Gly
NM_000194.3:c.200T>G MANE Select NP_000185.1:p.Val67Gly