Canonical Allele Identifier: CA397087855

Gene: APRT

Linked Data

• MyVariant Identifiers: chr16:g.88876516T>A (hg19) ; chr16:g.88810108T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810108T>A , CM000678.2:g.88810108T>A	GRCh38
NC_000016.9:g.88876516T>A , CM000678.1:g.88876516T>A	GRCh37
NC_000016.8:g.87404017T>A	NCBI36
NG_008013.1:g.6827A>T
NG_028266.1:g.11331T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.362A>T MANE Select	ENSP00000367615.3:p.Gln121Leu
ENST00000378364.7:c.362A>T	ENSP00000367615.3:p.Gln121Leu
ENST00000426324.6:c.362A>T	ENSP00000397007.2:p.Gln121Leu
ENST00000562464.1:n.372A>T
ENST00000563655.5:c.281A>T	ENSP00000456012.1:p.Gln94Leu
ENST00000567057.5:n.161A>T
ENST00000567391.5:c.*36A>T	ENSP00000457964.1:n.*36A>T
ENST00000567713.5:c.321+315A>T	ENSP00000455749.1:n.321+315A>T
ENST00000568319.5:c.*36A>T	ENSP00000456905.1:n.*36A>T
ENST00000568575.1:n.291A>T
ENST00000569616.1:c.360A>T
NM_000485.2:c.362A>T	NP_000476.1:p.Gln121Leu
NM_001030018.1:c.362A>T	NP_001025189.1:p.Gln121Leu
NM_000485.3:c.362A>T MANE Select	NP_000476.1:p.Gln121Leu
NM_001030018.2:c.362A>T	NP_001025189.1:p.Gln121Leu