Canonical Allele Identifier: CA2694742223
Gene: HPRT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134475076C>T , CM000685.2:g.134475076C>T GRCh38
NC_000023.10:g.133609106C>T , CM000685.1:g.133609106C>T GRCh37
NC_000023.9:g.133436772C>T NCBI36
NG_012329.1:g.19932C>T
NG_012329.2:g.19932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298556.8:c.135-105C>T MANE Select ENSP00000298556.7:n.135-105C>T
ENST00000298556.7:c.135-105C>T ENSP00000298556.7:n.135-105C>T
ENST00000462974.5:n.293-105C>T
ENST00000475720.1:n.93-105C>T
NM_000194.2:c.135-105C>T NP_000185.1:n.135-105C>T
XM_011531328.1:c.153-105C>T XP_011529630.1:n.153-105C>T
NM_000194.3:c.135-105C>T MANE Select NP_000185.1:n.135-105C>T