Canonical Allele Identifier: CA2459741105

Gene: HPRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134486477A= , CM000685.2:g.134486477A=	GRCh38
NC_000023.10:g.133620507A= , CM000685.1:g.133620507A=	GRCh37
NC_000023.9:g.133448173A=	NCBI36
NG_012329.1:g.31333A=
NG_012329.2:g.31333A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298556.8:c.331A= MANE Select	ENSP00000298556.7:p.Thr111=
ENST00000298556.7:c.331A=	ENSP00000298556.7:p.Thr111=
ENST00000462974.5:n.489A=
ENST00000475720.1:n.289A=
NM_000194.2:c.331A=	NP_000185.1:p.Thr111=
XM_011531328.1:c.349A=	XP_011529630.1:p.Thr117=
NM_000194.3:c.331A= MANE Select	NP_000185.1:p.Thr111=