Canonical Allele Identifier: CA397088047

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876549A>T (hg19) ; chr16:g.88810141A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810141A>T , CM000678.2:g.88810141A>T	GRCh38
NC_000016.9:g.88876549A>T , CM000678.1:g.88876549A>T	GRCh37
NC_000016.8:g.87404050A>T	NCBI36
NG_008013.1:g.6794T>A
NG_028266.1:g.11364A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378364.8:c.329T>A MANE Select	ENSP00000367615.3:p.Leu110Gln
ENST00000378364.7:c.329T>A	ENSP00000367615.3:p.Leu110Gln
ENST00000426324.6:c.329T>A	ENSP00000397007.2:p.Leu110Gln
ENST00000562464.1:n.339T>A
ENST00000563655.5:c.248T>A	ENSP00000456012.1:p.Leu83Gln
ENST00000567057.5:n.128T>A
ENST00000567391.5:c.*3T>A	ENSP00000457964.1:n.*3T>A
ENST00000567713.5:c.321+282T>A	ENSP00000455749.1:n.321+282T>A
ENST00000568319.5:c.*3T>A	ENSP00000456905.1:n.*3T>A
ENST00000568575.1:n.258T>A
ENST00000569616.1:c.327T>A
NM_000485.2:c.329T>A	NP_000476.1:p.Leu110Gln
NM_001030018.1:c.329T>A	NP_001025189.1:p.Leu110Gln
NM_000485.3:c.329T>A MANE Select	NP_000476.1:p.Leu110Gln
NM_001030018.2:c.329T>A	NP_001025189.1:p.Leu110Gln