Canonical Allele Identifier: CA2841422809

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809638del , CM000678.2:g.88809638del	GRCh38
NC_000016.9:g.88876046del , CM000678.1:g.88876046del	GRCh37
NC_000016.8:g.87403547del	NCBI36
NG_008013.1:g.7297del
NG_028266.1:g.10861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*60del MANE Select	ENSP00000367615.3:n.*60del
ENST00000378364.7:c.*60del	ENSP00000367615.3:n.*60del
ENST00000426324.6:c.*64del	ENSP00000397007.2:n.*64del
ENST00000563655.5:c.*60del	ENSP00000456012.1:n.*60del
ENST00000567057.5:n.268del
ENST00000567391.5:c.*277del	ENSP00000457964.1:n.*277del
ENST00000567713.5:c.322-103del	ENSP00000455749.1:n.322-103del
ENST00000568319.5:c.*143del	ENSP00000456905.1:n.*143del
ENST00000569616.1:c.668del
NM_000485.2:c.*60del	NP_000476.1:n.*60del
NM_001030018.1:c.*64del	NP_001025189.1:n.*64del
NM_000485.3:c.*60del MANE Select	NP_000476.1:n.*60del
NM_001030018.2:c.*64del	NP_001025189.1:n.*64del