Canonical Allele Identifier: CA658509620
Gene: HPRT1 HGNC NCBI

Linked Data

COSMIC: COSN22554545
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475147A>G , CM000685.2:g.134475147A>G GRCh38
NC_000023.10:g.133609177A>G , CM000685.1:g.133609177A>G GRCh37
NC_000023.9:g.133436843A>G NCBI36
NG_012329.1:g.20003A>G
NG_012329.2:g.20003A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298556.8:c.135-34A>G MANE Select ENSP00000298556.7:n.135-34A>G
ENST00000298556.7:c.135-34A>G ENSP00000298556.7:n.135-34A>G
ENST00000462974.5:n.293-34A>G
ENST00000475720.1:n.93-34A>G
NM_000194.2:c.135-34A>G NP_000185.1:n.135-34A>G
XM_011531328.1:c.153-34A>G XP_011529630.1:n.153-34A>G
NM_000194.3:c.135-34A>G MANE Select NP_000185.1:n.135-34A>G
Search 100 bp 5'
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