Canonical Allele Identifier: CA2241307815

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809652T= , CM000678.2:g.88809652T=	GRCh38
NC_000016.9:g.88876060T= , CM000678.1:g.88876060T=	GRCh37
NC_000016.8:g.87403561T=	NCBI36
NG_008013.1:g.7283A=
NG_028266.1:g.10875T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*46A= MANE Select	ENSP00000367615.3:n.*46A=
ENST00000378364.7:c.*46A=	ENSP00000367615.3:n.*46A=
ENST00000426324.6:c.*50A=	ENSP00000397007.2:n.*50A=
ENST00000563655.5:c.*46A=	ENSP00000456012.1:n.*46A=
ENST00000567057.5:n.254A=
ENST00000567391.5:c.*263A=	ENSP00000457964.1:n.*263A=
ENST00000567713.5:c.322-117A=	ENSP00000455749.1:n.322-117A=
ENST00000568319.5:c.*129A=	ENSP00000456905.1:n.*129A=
ENST00000569616.1:c.654A=
NM_000485.2:c.*46A=	NP_000476.1:n.*46A=
NM_001030018.1:c.*50A=	NP_001025189.1:n.*50A=
NM_000485.3:c.*46A= MANE Select	NP_000476.1:n.*46A=
NM_001030018.2:c.*50A=	NP_001025189.1:n.*50A=