Canonical Allele Identifier: CA2241308370
Gene: APRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88810453_88810455delinsCAG , CM000678.2:g.88810453_88810455delinsCAG GRCh38
NC_000016.9:g.88876861_88876863delinsCAG , CM000678.1:g.88876861_88876863delinsCAG GRCh37
NC_000016.8:g.87404362_87404364delinsCAG NCBI36
NG_008013.1:g.6480_6482delinsCTG
NG_028266.1:g.11676_11678delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000378364.8:c.289_291delinsCTG MANE Select ENSP00000367615.3:p.Leu97=
ENST00000378364.7:c.289_291delinsCTG ENSP00000367615.3:p.Leu97=
ENST00000426324.6:c.289_291delinsCTG ENSP00000397007.2:p.Leu97=
ENST00000562464.1:n.332-307_332-305delinsCTG
ENST00000563655.5:c.241-307_241-305delinsCTG ENSP00000456012.1:n.241-307_241-305delins...
ENST00000567391.5:c.188-307_188-305delinsCTG ENSP00000457964.1:n.188-307_188-305delins...
ENST00000567713.5:c.289_291delinsCTG ENSP00000455749.1:p.Leu97=
ENST00000568319.5:c.188-307_188-305delinsCTG ENSP00000456905.1:n.188-307_188-305delins...
ENST00000569616.1:c.287_289delinsCTG
NM_000485.2:c.289_291delinsCTG NP_000476.1:p.Leu97=
NM_001030018.1:c.289_291delinsCTG NP_001025189.1:p.Leu97=
NM_000485.3:c.289_291delinsCTG MANE Select NP_000476.1:p.Leu97=
NM_001030018.2:c.289_291delinsCTG NP_001025189.1:p.Leu97=