Canonical Allele Identifier: CA497086009

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876518T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810110T>A , CM000678.2:g.88810110T>A	GRCh38
NC_000016.9:g.88876518T>A , CM000678.1:g.88876518T>A	GRCh37
NC_000016.8:g.87404019T>A	NCBI36
NG_008013.1:g.6825A>T
NG_028266.1:g.11333T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.360A>T MANE Select	ENSP00000367615.3:p.Gly120=
ENST00000378364.7:c.360A>T	ENSP00000367615.3:p.Gly120=
ENST00000426324.6:c.360A>T	ENSP00000397007.2:p.Gly120=
ENST00000562464.1:n.370A>T
ENST00000563655.5:c.279A>T	ENSP00000456012.1:p.Gly93=
ENST00000567057.5:n.159A>T
ENST00000567391.5:c.*34A>T	ENSP00000457964.1:n.*34A>T
ENST00000567713.5:c.321+313A>T	ENSP00000455749.1:n.321+313A>T
ENST00000568319.5:c.*34A>T	ENSP00000456905.1:n.*34A>T
ENST00000568575.1:n.289A>T
ENST00000569616.1:c.358A>T
NM_000485.2:c.360A>T	NP_000476.1:p.Gly120=
NM_001030018.1:c.360A>T	NP_001025189.1:p.Gly120=
NM_000485.3:c.360A>T MANE Select	NP_000476.1:p.Gly120=
NM_001030018.2:c.360A>T	NP_001025189.1:p.Gly120=