Canonical Allele Identifier: CA2241307830

Gene: APRT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88809682C= , CM000678.2:g.88809682C=	GRCh38
NC_000016.9:g.88876090C= , CM000678.1:g.88876090C=	GRCh37
NC_000016.8:g.87403591C=	NCBI36
NG_008013.1:g.7253G=
NG_028266.1:g.10905C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378364.8:c.*16G= MANE Select	ENSP00000367615.3:n.*16G=
ENST00000378364.7:c.*16G=	ENSP00000367615.3:n.*16G=
ENST00000426324.6:c.*20G=	ENSP00000397007.2:n.*20G=
ENST00000563655.5:c.*16G=	ENSP00000456012.1:n.*16G=
ENST00000567057.5:n.224G=
ENST00000567391.5:c.*233G=	ENSP00000457964.1:n.*233G=
ENST00000567713.5:c.322-147G=	ENSP00000455749.1:n.322-147G=
ENST00000568319.5:c.*99G=	ENSP00000456905.1:n.*99G=
ENST00000568575.1:n.488G=
ENST00000569616.1:c.624G=
NM_000485.2:c.*16G=	NP_000476.1:n.*16G=
NM_001030018.1:c.*20G=	NP_001025189.1:n.*20G=
NM_000485.3:c.*16G= MANE Select	NP_000476.1:n.*16G=
NM_001030018.2:c.*20G=	NP_001025189.1:n.*20G=