Canonical Allele Identifier: CA2241308376
Gene: APRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88810458T= , CM000678.2:g.88810458T= GRCh38
NC_000016.9:g.88876866T= , CM000678.1:g.88876866T= GRCh37
NC_000016.8:g.87404367T= NCBI36
NG_008013.1:g.6477A=
NG_028266.1:g.11681T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378364.8:c.286A= MANE Select ENSP00000367615.3:p.Thr96=
ENST00000378364.7:c.286A= ENSP00000367615.3:p.Thr96=
ENST00000426324.6:c.286A= ENSP00000397007.2:p.Thr96=
ENST00000562464.1:n.332-310A=
ENST00000563655.5:c.241-310A= ENSP00000456012.1:n.241-310A=
ENST00000567391.5:c.188-310A= ENSP00000457964.1:n.188-310A=
ENST00000567713.5:c.286A= ENSP00000455749.1:p.Thr96=
ENST00000568319.5:c.188-310A= ENSP00000456905.1:n.188-310A=
ENST00000569616.1:c.284A=
NM_000485.2:c.286A= NP_000476.1:p.Thr96=
NM_001030018.1:c.286A= NP_001025189.1:p.Thr96=
NM_000485.3:c.286A= MANE Select NP_000476.1:p.Thr96=
NM_001030018.2:c.286A= NP_001025189.1:p.Thr96=