Canonical Allele Identifier: CA397088002

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876540T>G (hg19) ; chr16:g.88810132T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810132T>G , CM000678.2:g.88810132T>G	GRCh38
NC_000016.9:g.88876540T>G , CM000678.1:g.88876540T>G	GRCh37
NC_000016.8:g.87404041T>G	NCBI36
NG_008013.1:g.6803A>C
NG_028266.1:g.11355T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.338A>C MANE Select	ENSP00000367615.3:p.Gln113Pro
ENST00000378364.7:c.338A>C	ENSP00000367615.3:p.Gln113Pro
ENST00000426324.6:c.338A>C	ENSP00000397007.2:p.Gln113Pro
ENST00000562464.1:n.348A>C
ENST00000563655.5:c.257A>C	ENSP00000456012.1:p.Gln86Pro
ENST00000567057.5:n.137A>C
ENST00000567391.5:c.*12A>C	ENSP00000457964.1:n.*12A>C
ENST00000567713.5:c.321+291A>C	ENSP00000455749.1:n.321+291A>C
ENST00000568319.5:c.*12A>C	ENSP00000456905.1:n.*12A>C
ENST00000568575.1:n.267A>C
ENST00000569616.1:c.336A>C
NM_000485.2:c.338A>C	NP_000476.1:p.Gln113Pro
NM_001030018.1:c.338A>C	NP_001025189.1:p.Gln113Pro
NM_000485.3:c.338A>C MANE Select	NP_000476.1:p.Gln113Pro
NM_001030018.2:c.338A>C	NP_001025189.1:p.Gln113Pro