Canonical Allele Identifier: CA397090630

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88811658T>C , CM000678.2:g.88811658T>C	GRCh38
NC_000016.9:g.88878066T>C , CM000678.1:g.88878066T>C	GRCh37
NC_000016.8:g.87405567T>C	NCBI36
NG_008013.1:g.5277A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000485.3:c.81-2A>G MANE Select	NP_000476.1:n.81-2A>G
ENST00000378364.8:c.81-2A>G MANE Select	ENSP00000367615.3:n.81-2A>G
NM_000485.2:c.81-2A>G	NP_000476.1:n.81-2A>G
NM_001030018.1:c.81-2A>G	NP_001025189.1:n.81-2A>G
NM_001030018.2:c.81-2A>G	NP_001025189.1:n.81-2A>G
ENST00000378364.7:c.81-2A>G	ENSP00000367615.3:n.81-2A>G
ENST00000426324.6:c.81-2A>G	ENSP00000397007.2:n.81-2A>G
ENST00000562464.1:n.223A>G
ENST00000563655.5:c.81-2A>G	ENSP00000456012.1:n.81-2A>G
ENST00000564858.1:n.102-2A>G
ENST00000567391.5:c.81-2A>G	ENSP00000457964.1:n.81-2A>G
ENST00000567713.5:c.81-2A>G	ENSP00000455749.1:n.81-2A>G
ENST00000568319.5:c.81-2A>G	ENSP00000456905.1:n.81-2A>G
ENST00000569616.1:c.79-2A>G