Canonical Allele Identifier: CA397088156
Gene: APRT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88810425T>A , CM000678.2:g.88810425T>A GRCh38
NC_000016.9:g.88876833T>A , CM000678.1:g.88876833T>A GRCh37
NC_000016.8:g.87404334T>A NCBI36
NG_008013.1:g.6510A>T
NG_028266.1:g.11648T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378364.8:c.319A>T MANE Select ENSP00000367615.3:p.Lys107Ter
ENST00000378364.7:c.319A>T ENSP00000367615.3:p.Lys107Ter
ENST00000426324.6:c.319A>T ENSP00000397007.2:p.Lys107Ter
ENST00000562464.1:n.332-277A>T
ENST00000563655.5:c.241-277A>T ENSP00000456012.1:n.241-277A>T
ENST00000567391.5:c.188-277A>T ENSP00000457964.1:n.188-277A>T
ENST00000567713.5:c.319A>T ENSP00000455749.1:p.Lys107Ter
ENST00000568319.5:c.188-277A>T ENSP00000456905.1:n.188-277A>T
ENST00000569616.1:c.317A>T
NM_000485.2:c.319A>T NP_000476.1:p.Lys107Ter
NM_001030018.1:c.319A>T NP_001025189.1:p.Lys107Ter
NM_000485.3:c.319A>T MANE Select NP_000476.1:p.Lys107Ter
NM_001030018.2:c.319A>T NP_001025189.1:p.Lys107Ter