Canonical Allele Identifier: CA2808070173

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88810161_88810162insGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCGAACA , CM000678.2:g.88810161_88810162insGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCGAACA	GRCh38
NC_000016.9:g.88876569_88876570insGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCGAACA , CM000678.1:g.88876569_88876570insGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCGAACA	GRCh37
NC_000016.8:g.87404070_87404071insGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCGAACA	NCBI36
NG_008013.1:g.6773_6774insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC
NG_028266.1:g.11384_11385insGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCGAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC MANE Select	ENSP00000367615.3:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTC...
ENST00000378364.7:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	ENSP00000367615.3:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTC...
ENST00000426324.6:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	ENSP00000397007.2:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTC...
ENST00000562464.1:n.332-14_332-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC
ENST00000563655.5:c.241-14_241-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	ENSP00000456012.1:n.241-14_241-13insTGTTCGCCAGGATGGTCTCGATCTC...
ENST00000567057.5:n.107_108insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC
ENST00000567391.5:c.188-14_188-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	ENSP00000457964.1:n.188-14_188-13insTGTTCGCCAGGATGGTCTCGATCTC...
ENST00000567713.5:c.321+261_321+262insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	ENSP00000455749.1:n.321+261_321+262insTGTTCGCCAGGATGGTCTCGATC...
ENST00000568319.5:c.188-14_188-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	ENSP00000456905.1:n.188-14_188-13insTGTTCGCCAGGATGGTCTCGATCTC...
ENST00000568575.1:n.237_238insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC
ENST00000569616.1:c.320-14_320-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC
NM_000485.2:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	NP_000476.1:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACC...
NM_001030018.1:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	NP_001025189.1:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTG...
NM_000485.3:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC MANE Select	NP_000476.1:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACC...
NM_001030018.2:c.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCCACCTTGGCCTCC	NP_001025189.1:n.322-14_322-13insTGTTCGCCAGGATGGTCTCGATCTCTTG...