Canonical Allele Identifier: CA2241307798
Gene: APRT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88809622C= , CM000678.2:g.88809622C= GRCh38
NC_000016.9:g.88876030C= , CM000678.1:g.88876030C= GRCh37
NC_000016.8:g.87403531C= NCBI36
NG_008013.1:g.7313G=
NG_028266.1:g.10845C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378364.8:c.*76G= MANE Select ENSP00000367615.3:n.*76G=
ENST00000378364.7:c.*76G= ENSP00000367615.3:n.*76G=
ENST00000426324.6:c.*80G= ENSP00000397007.2:n.*80G=
ENST00000563655.5:c.*76G= ENSP00000456012.1:n.*76G=
ENST00000567057.5:n.284G=
ENST00000567391.5:c.*293G= ENSP00000457964.1:n.*293G=
ENST00000567713.5:c.322-87G= ENSP00000455749.1:n.322-87G=
ENST00000568319.5:c.*159G= ENSP00000456905.1:n.*159G=
ENST00000569616.1:c.684G=
NM_000485.2:c.*76G= NP_000476.1:n.*76G=
NM_001030018.1:c.*80G= NP_001025189.1:n.*80G=
NM_000485.3:c.*76G= MANE Select NP_000476.1:n.*76G=
NM_001030018.2:c.*80G= NP_001025189.1:n.*80G=