Canonical Allele Identifier: CA2241307836

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809687A= , CM000678.2:g.88809687A=	GRCh38
NC_000016.9:g.88876095A= , CM000678.1:g.88876095A=	GRCh37
NC_000016.8:g.87403596A=	NCBI36
NG_008013.1:g.7248T=
NG_028266.1:g.10910A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*11T= MANE Select	ENSP00000367615.3:n.*11T=
ENST00000378364.7:c.*11T=	ENSP00000367615.3:n.*11T=
ENST00000426324.6:c.*15T=	ENSP00000397007.2:n.*15T=
ENST00000563655.5:c.*11T=	ENSP00000456012.1:n.*11T=
ENST00000567057.5:n.219T=
ENST00000567391.5:c.*228T=	ENSP00000457964.1:n.*228T=
ENST00000567713.5:c.322-152T=	ENSP00000455749.1:n.322-152T=
ENST00000568319.5:c.*94T=	ENSP00000456905.1:n.*94T=
ENST00000568575.1:n.483T=
ENST00000569616.1:c.619T=
NM_000485.2:c.*11T=	NP_000476.1:n.*11T=
NM_001030018.1:c.*15T=	NP_001025189.1:n.*15T=
NM_000485.3:c.*11T= MANE Select	NP_000476.1:n.*11T=
NM_001030018.2:c.*15T=	NP_001025189.1:n.*15T=