Canonical Allele Identifier: CA2694742227
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475078C>G , CM000685.2:g.134475078C>G GRCh38
NC_000023.10:g.133609108C>G , CM000685.1:g.133609108C>G GRCh37
NC_000023.9:g.133436774C>G NCBI36
NG_012329.1:g.19934C>G
NG_012329.2:g.19934C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-103C>G MANE Select ENSP00000298556.7:n.135-103C>G
ENST00000298556.7:c.135-103C>G ENSP00000298556.7:n.135-103C>G
ENST00000462974.5:n.293-103C>G
ENST00000475720.1:n.93-103C>G
NM_000194.2:c.135-103C>G NP_000185.1:n.135-103C>G
XM_011531328.1:c.153-103C>G XP_011529630.1:n.153-103C>G
NM_000194.3:c.135-103C>G MANE Select NP_000185.1:n.135-103C>G