Canonical Allele Identifier: CA2241308100

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810068_88810078delinsACCACCAGTGG , CM000678.2:g.88810068_88810078delinsACCACCAGTGG	GRCh38
NC_000016.9:g.88876476_88876486delinsACCACCAGTGG , CM000678.1:g.88876476_88876486delinsACCACCAGTGG	GRCh37
NC_000016.8:g.87403977_87403987delinsACCACCAGTGG	NCBI36
NG_008013.1:g.6857_6867delinsCCACTGGTGGT
NG_028266.1:g.11291_11301delinsACCACCAGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.392_400+2delinsCCACTGGTGGT
ENST00000378364.7:c.392_400+2delinsCCACTGGTGGT
ENST00000426324.6:c.392_400+2delinsCCACTGGTGGT
ENST00000562464.1:n.402_410+2delinsCCACTGGTGGT
ENST00000563655.5:c.311_319+2delinsCCACTGGTGGT
ENST00000567057.5:n.191_199+2delinsCCACTGGTGGT
ENST00000567391.5:c.*66_*74+2delinsCCACTGGTGGT
ENST00000567713.5:c.321+345_321+355delinsCCACTGGTGGT	ENSP00000455749.1:n.321+345_321+355delinsCCACTGGTGGT
ENST00000568319.5:c.*66_*74+2delinsCCACTGGTGGT
ENST00000568575.1:n.321_329+2delinsCCACTGGTGGT
ENST00000569616.1:c.390_398+2delinsCCACTGGTGGT
NM_000485.2:c.392_400+2delinsCCACTGGTGGT
NM_001030018.1:c.392_400+2delinsCCACTGGTGGT
NM_000485.3:c.392_400+2delinsCCACTGGTGGT
NM_001030018.2:c.392_400+2delinsCCACTGGTGGT