Canonical Allele Identifier: CA2241308371
Gene: APRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88810453C= , CM000678.2:g.88810453C= GRCh38
NC_000016.9:g.88876861C= , CM000678.1:g.88876861C= GRCh37
NC_000016.8:g.87404362C= NCBI36
NG_008013.1:g.6482G=
NG_028266.1:g.11676C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378364.8:c.291G= MANE Select ENSP00000367615.3:p.Leu97=
ENST00000378364.7:c.291G= ENSP00000367615.3:p.Leu97=
ENST00000426324.6:c.291G= ENSP00000397007.2:p.Leu97=
ENST00000562464.1:n.332-305G=
ENST00000563655.5:c.241-305G= ENSP00000456012.1:n.241-305G=
ENST00000567391.5:c.188-305G= ENSP00000457964.1:n.188-305G=
ENST00000567713.5:c.291G= ENSP00000455749.1:p.Leu97=
ENST00000568319.5:c.188-305G= ENSP00000456905.1:n.188-305G=
ENST00000569616.1:c.289G=
NM_000485.2:c.291G= NP_000476.1:p.Leu97=
NM_001030018.1:c.291G= NP_001025189.1:p.Leu97=
NM_000485.3:c.291G= MANE Select NP_000476.1:p.Leu97=
NM_001030018.2:c.291G= NP_001025189.1:p.Leu97=