Canonical Allele Identifier: CA2241307801

Gene: APRT

Linked Data

• dbSNP Id: rs1909027626

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809624T>C , CM000678.2:g.88809624T>C	GRCh38
NC_000016.9:g.88876032T>C , CM000678.1:g.88876032T>C	GRCh37
NC_000016.8:g.87403533T>C	NCBI36
NG_008013.1:g.7311A>G
NG_028266.1:g.10847T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*74A>G MANE Select	ENSP00000367615.3:n.*74A>G
ENST00000378364.7:c.*74A>G	ENSP00000367615.3:n.*74A>G
ENST00000426324.6:c.*78A>G	ENSP00000397007.2:n.*78A>G
ENST00000563655.5:c.*74A>G	ENSP00000456012.1:n.*74A>G
ENST00000567057.5:n.282A>G
ENST00000567391.5:c.*291A>G	ENSP00000457964.1:n.*291A>G
ENST00000567713.5:c.322-89A>G	ENSP00000455749.1:n.322-89A>G
ENST00000568319.5:c.*157A>G	ENSP00000456905.1:n.*157A>G
ENST00000569616.1:c.682A>G
NM_000485.2:c.*74A>G	NP_000476.1:n.*74A>G
NM_001030018.1:c.*78A>G	NP_001025189.1:n.*78A>G
NM_000485.3:c.*74A>G MANE Select	NP_000476.1:n.*74A>G
NM_001030018.2:c.*78A>G	NP_001025189.1:n.*78A>G